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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927283Generated: November 1, 2026

Benzenepropanoic acid → HCID 12740364, compound

https://huagongshe.com/reaction/1927283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenepropanoic acidHCID 107—
ReactantCyanoacetic acidHCID 9740—
ReactantBenzenepropanoyl chlorideHCID 64801—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventThionyl ChlorideHCID 24386—
ProductHCID 12740364HCID 12740364—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of cyanoacetic acid (1.0 g, 11.8 mmol) in tetrahydrofuran (20 mL) was cooled to −78° C. and treated with 1.6 M n-butyl lithium in hexanes (14.7 mL, 23.5 mmol). The mixture was warmed to −20° C. over 2 hours, cooled to −78° C. and treated with 3-phenylpropionyl chloride (prepared by refluxing a solution of 3-phenylpropionic acid (1.0 g, 6.7 mmol) in thionyl chloride (4 mL) for 3 hours, evaporating and drying). The mixture was stirred at −78° C. for 1 hour and 20% hydrochloric acid added until the pH=3. The mixture was diluted with diethyl ether, washed with saturated sodium bicarbonate, and the organic layer separated and concentrated. The crude product was purified by flash chromatography on silica gel using 0-50% ethyl acetate/hexanes to provide the title compound. MS (ESI) m/e 191 (M+H+NH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183250B2
Source datasetuspto-grants-2012_05
ORD IDord-76a61b00b8424ba59897327eaa48cb5f
Source noteuspto-grants-2012_05