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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593262Generated: October 26, 2026

Hydrochloric Acid → 3-Phenylbutyric acid

https://huagongshe.com/reaction/593262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromobenzeneHCID 7961—
ReactantCrotonic AcidHCID 637090—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Phenylbutyric acidHCID 2072460%

Reaction Conditions

Temperature-78 °C

Reaction Steps

As presented in the following reaction formula, n-butyllithium (n-BuLi; 428 mL, 1.07 mol) was added dropwise at −78° C. to −65° C. to a mixture of bromobenzene (166 g, 1.07 mol) in tetrahydrofuran (THF; 500 mL), followed by stirring at −78° C. for 0.5 hours. Then, (E)-but-2-enoic acid (46 g, 0.53 mol) was added dropwise to the resulting mixture. After the completion of reaction, the mixture was treated with hydrochloric acid so that the pH thereof was adjusted to 1.0, and then extracted twice with 500 mL of dichloromethane (DCM). The combined organic phase was dried and concentrated with magnesium sulfate to give a crude product, which was purified by column chromatography (using 300 g of silica gel (product of Merck Co., Ltd.) to give 3-phenylbutanoic acid (52 g, yield: 60%) as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242928B2
Source datasetuspto-grants-2016_01
ORD IDord-d6fb234995ba403ea1a361ffbcd8273f
Source noteuspto-grants-2016_01