Jing
Li
a,
Liqun
Jin
a,
Chao
Liu
a and
Aiwen
Lei
*ab
aCollege of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, Hubei, P. R. China. E-mail: aiwenlei@whu.edu.cn
bNational Research Center for Carbohydrate Synthesis, Jiangxi Normal University, Nanchang 330022, Jiangxi, P. R. China
First published on 19th December 2013
Transmetalation is the rate-limiting step in Negishi coupling: in a live “Pd-catalyzed Negishi coupling of ArI with Ar′ZnX”, the transmetalation was assigned as the rate-limiting step through kinetic investigation. Quantitative measurements of the transmetalation of ArZnX with [Ar–Pd–X] from this live Pd-catalyzed coupling reaction were obtained and the activation enthalpy is 11.3 kcal mol−1.
The Pd-catalyzed Negishi coupling is generally believed to follow three fundamental steps: oxidative addition, transmetalation and reductive elimination.8 Among these three steps, the transmetalation occurs between an organozinc reagent and [RPdX] species, which is one of the most important ways to introduce σ-bonded carbon atoms into the coordination sphere of palladium and furnish the [R–Pd–R′] species.2,9 Obviously, revealing mechanistic insights into the transmetalation step of Negishi coupling is significant and urgent for better conducting these transformations in chemical synthesis.10–13
However, mechanistic studies on the transmetalation of Negishi coupling are relatively less reported compared with Suzuki coupling and Stille coupling,14–30 especially the transmetalation of the Ar1ZnX reagent with Ar2PdX species from “live” Pd-catalyzed biaryl-syntheses (Ar1–Ar2). In recent years, mechanistic studies on transmetalation of organozinc reagents have drawn more and more attention. For example, Espinet and coworkers continually reported their understanding of the transmetalation step of [Ralkyl–Pd–X] with MeZnX/Me2Zn through stoichiometric experiments under low temperature with special ligands and substrates.7,31,32 However, the stoichiometric experiments would become problematic as the transmetalation of [R–Pd–X] with an organozinc reagent is too rapid to be probed under “live” Negishi coupling reaction conditions. Therefore, the challenge remains in gaining mechanistic insights into the transmetalation of Negishi coupling under live catalytic reaction conditions. Herein, we document our recent results in quantitative measurements of the transmetalation of Ar1ZnX with [Ar2–Pd–X] through kinetic investigations from a live Pd-catalyzed Negishi coupling.
Our initial studies commenced from the curiosity about the real catalytic capability of Pd(OAc)2 in Negishi coupling. The Pd-catalyzed cross-coupling between ethyl 4-iodobenzoate (1) and p-MeC6H4ZnCl (2) using Pd(OAc)2 as the catalyst precursor was investigated. The reactions could proceed smoothly in quantitative yields with both 5 mol% and 1 mol% catalyst loadings. The TONs were 20 and 100, respectively. We also found that these reactions were very rapid (within 60 seconds) and clearly there was Pd-black formation shown in Fig. 1A when 5 mol% or 1 mol% Pd(OAc)2 was employed. However, when 0.1 mol% Pd(OAc)2 was employed, the reaction could proceed smoothly and no Pd-black was observed. It is very interesting that the TONs could reach up to 290000 at 10 °C when the concentration of Pd was decreased (Fig. 1A). The continuous increase of TONs indicated the powerful catalytic potential.
To our great surprise, when kinetic studies were performed using in situ IR, a strange [catalysts]-kinetic dependence was observed. As shown in Fig. 1B, when the reaction was performed using a lower concentration of the Pd catalyst (<8.0 × 10−6 M), the initial rates exhibited a positive dependence on the concentration of the catalyst. However, when the reaction was performed using a higher concentration of the Pd catalyst (≥8.0 × 10−6 M), a negative dependence on the concentration of the catalyst was determined. The impressive efficiency and unpredictable kinetic behavior in this Pd-catalyzed Negishi coupling inspired us to further probe the transformation in detail.
With this Pd-catalyzed cross-coupling between 1 and 2 as a model, further kinetic investigations were carried out. As mentioned above, when [Pd] ≥ 8.0 × 10−6 M, increasing the concentration of Pd would result in lower reaction rates, revealing that some Pd species might be out of the catalytic cycle and decompose under these conditions. Thus, the reaction performed at high concentration of Pd could not be employed for kinetic studies. Subsequently, reactions with different concentrations of Pd at 10 °C ([Pd] < 8.0 × 10−6 M) were carried out. As shown in Fig. 2, when plotting the initial rates vs. [Pd], a linear relationship could be determined, suggesting that the reaction exhibits first-order kinetic behavior on the concentration of Pd under those conditions. In this regard, the following kinetic experiments were performed under the obtained Pd concentration range ([Pd] ≤ 7.0 × 10−6 M).
Fig. 2 Plotting initial rates vs. [Pd]. Reaction conditions: 1 (0.25 M in THF), 2 (0.34 M in THF, 4.0 mL), Pd(OAc)2 (8.2 × 10−7–7.2 × 10−6 M in THF), 10 °C. |
The subsequent reactions with different concentrations of ArI were performed and monitored by in situ IR. As shown in Fig. 3, the reactions show similar reaction rates, suggesting that the reactions exhibited zero order dependence on [ArI]. Meanwhile, the kinetic behavior of ArZnCl was examined. It was observed that plotting initial rates vs. [ArZnCl] yielded a line, revealing that the reaction exhibited a first-order dependence on [ArZnCl] (Fig. 4).
Fig. 3 Plotting initial rates vs. [ArI]. Reaction conditions: 1 (0.073–0.26 M in THF), 2 (0.33 M in THF, 4.0 mL), Pd(OAc)2 (5.2 × 10−6 M in THF), −10 °C. |
Fig. 4 Plotting initial rates vs. [ArZnCl]. Reaction conditions: 1 (0.082 M in THF), 2 (0.17–0.35 M in THF, 6.0 mL), Pd(OAc)2 (6.6 × 10−6 M in THF), −10 °C. |
On the basis of the kinetic results above, the rate law of this Pd-catalyzed cross-coupling between ethyl 4-iodobenzoate and p-Me C6H4ZnCl could be derived as: rate = k × [Pd] × [ArZnCl]. Zero-order kinetic dependence on [1] and first-order dependence on [2] suggest that transmetalation might be the rate-limiting step.
Subsequently, the rates of this Negishi coupling using different para-substituted (R = MeO, Me, H, Cl) arylzinc reagents were measured. Arylzinc reagents with electron-donating substituents reacted faster than electron-deficient arylzinc reagents. As shown in Fig. 5, a linear free energy relationship was observed with a calculated ρ-value of −1.07. The negative ρ-value signified that in the rate limiting step, arylzinc should be involved in the transition state and a positive charge buildup exists in the phenyl ring of arylzinc, further supporting that the transmetalation is the rate-limiting step.
Fig. 5 Hammett plot of Pd-catalyzed Negishi coupling between 1 and ArZnX. Reaction conditions: 1 (0.12 M in THF), ArZnX (0.31 M in THF, 4.0 mL), Pd(OAc)2 (5.2 × 10−6 M in THF), −10 °C. |
Having confirmed that transmetalation was the rate-limiting step, we were allowed to gain further understanding of the transmetalation of arylzinc. Then the activation parameters were determined through Eyring analysis by measuring the reaction rates from −20 to 30 °C. As shown in Fig. 6, the activation enthalpy ΔH≠ was measured to be 11.3 kcal mol−1.
Fig. 6 Eyring plots of Pd-catalyzed Negishi coupling between 1 and 2. Reaction conditions: 1 (0.12 M in THF), 2 (0.25 M in THF, 4.0 mL), Pd(OAc)2 (5.2 × 10−6 M in THF), −20–30 °C. |
Footnote |
† Electronic supplementary information (ESI) available: Detailed experimental procedures and kinetic parameters detected by a Mettler Toledo ReactIR™ 15 spectrometer. See DOI: 10.1039/c3qo00021d |
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