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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273996Generated: October 25, 2026

3-(Bromomethyl)benzoic acid → 3-[2-Cyano-2-(3,4-dimethoxyphenyl)-2-[(4-methylphenyl)thio]ethyl]benzoic acid

https://huagongshe.com/reaction/273996

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Bromomethyl)benzoic acidHCID 245650—
Reactant3,4-Dimethoxy-alpha[(4-methylphenyl)thio]benzeneacetonitrileHCID 10542167—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-[2-Cyano-2-(3,4-dimethoxyphenyl)-2-[(4-methylphenyl)thio]ethyl]benzoic acidHCID 1059889785.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cold (-78° C.) solution of 1.86 g of 3,4-dimethoxy-α-[(4-methylphenyl)thio]benzene acetonitrile in 15 mL of tetrahydrofuran is added drop-wise a solution of 2.9 mL of n-butyl lithium (2.2 M) in hexane. This solution is stirred at -78° C. for 35 minutes. A solution of 0.67 g of m-carboxybenzyl bromide in 5 mL of anhydrous tetrahydrofuran is added drop-wise, stirred at -78° C. for 40 minutes and then at room temperature for 15 minutes. The mixture is quenched with water and extracted with ethyl acetate. The ethyl acetate extract is washed with brine, dried and filtered. The filtrate is evaporated in vacuo to yield a yellow oil. This oil is purified by flash chromatography using methylene chloride/methyl alcohol (95:5) to yield 1.15 g of the desired product as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387685
Source datasetuspto-grants-1995_02
ORD IDord-260917c3a7ef4014bb2b71352417c94a
Source noteuspto-grants-1995_02