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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641998Generated: October 29, 2026

Acetic Anhydride → HCID 59283848, compound

https://huagongshe.com/reaction/1641998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 54253994HCID 54253994—
SolventPyridineHCID 1049—
ProductHCID 59283848HCID 59283848—

Reaction Steps

A solution of methyl 4-hydroxy-3-allyl-5-methylbenzoate (157 mg) in pyridine (5 mL) was cooled in an ice-bath under a nitrogen atmosphere and treated with acetic anhydride (1 mL). The reaction was stirred in the ice-bath for one hour and was then warmed to room temperature for 4 hours. The solvent was then removed under reduced pressure and the residue was suspended in anhydrous toluene (5-10 mL) and evaporated to dryness. The crude product was dissolved in ethyl acetate (30 mL) and washed with saturated aqueous ammonium chloride. It was then dried over anhydrous magnesium sulfate, filtered and evaporated to dryness to give a brown oil. Yield=0.176 g (quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119422B2
Source datasetuspto-grants-2012_02
ORD IDord-0d2960827cf6420bb99d0cb53d8717ef
Source noteuspto-grants-2012_02