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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492347Generated: October 30, 2026

Benzoic acid, 4-(acetyloxy)- → 4-Acetoxy-l-(1-methylbutyloxycarbonyl)benzene

https://huagongshe.com/reaction/1492347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid, 4-(acetyloxy)-HCID 16865—
ReactantThionyl ChlorideHCID 24386—
Product4-Acetoxy-l-(1-methylbutyloxycarbonyl)benzeneHCID 1895013551.1%

Reaction Steps

4-Acetoxybenzoic acid (6.2 g) was added to 25 ml of thionyl chloride, and the reaction was conducted under reflux for 10 hours. After excess thionyl chloride was distilled off, 15 ml of pyridine and 90 ml of toluene were added. Two grams of optically active S-(+)-2-pentanol was added dropwise thereto. After the addition, the mixture was heated under reflux for 4 hours, left to cool and diluted with 500 ml of chloroform. The organic layer was washed with dilute hydrochloric acid, a 1N sodium hydroxide aqueous solution and water in this order, and dried with magnesium sulfate. Further, the solvent was evaporated to obtain 2.2 g of a final crude compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374375
Source datasetuspto-grants-1994_12
ORD IDord-7b277416a09149b0bf4bebb2c1badc26
Source noteuspto-grants-1994_12