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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300475Generated: October 25, 2026

Sodium bis(trimethylsilyl)amide → 3-(3-Cyano-phenyl)-2-methyl-propionic acid methyl ester

https://huagongshe.com/reaction/2300475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantMethyl 3-(3-cyanophenyl)propanoateHCID 20257048—
ReactantSodium bicarbonate waterHCID 86585896—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Cyano-phenyl)-2-methyl-propionic acid methyl esterHCID 5452302426.3%

Reaction Steps

To a solution of 3-(3-cyano-phenyl)-propionic acid methyl ester of Step A (220 mg, 1.16 mmol) in THF (5 mL) at −78° C. was added sodium bis(trimethylsilyl)amide (1 M in THF, 1.2 mL, 1.2 mmol). The reaction was stirred for 0.5 h and Mel (0.08 mL, 1.28 mmol) was added. After 1 h, a solution of saturated NaHCO3:water (1:1) was added and the reaction was warmed to room temperature. The aqueous solution was washed with CH2Cl2 (3×) and the combined organic solutions were dried (MgSO4), filtered, and concentrated. Medium pressure chromatography (6:1 hexanes:EtOAc) provided the title compound of Step B as a colorless oil (62 mg). 1H NMR (400 MHz, CDCl3) δ 7.50-7.34 (m, 4H), 3.62 (s, 3H), 3.01 (m, 1H), 2.71 (m, 2H), 1.16 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498172B1
Source datasetuspto-grants-2002_12
ORD IDord-a21535a9dbbe4ef8b90881c0b032750d
Source noteuspto-grants-2002_12