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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030424Generated: November 2, 2026

Acetic Anhydride → HCID 13605827, compound

https://huagongshe.com/reaction/1030424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13605826HCID 13605826—
SolventPyridineHCID 1049—
ProductHCID 13605827HCID 13605827—

Reaction Steps

A mixture of 1.7 g of 7-t-butyl-6-hydroxy-2-methyl-2-(4-nitrophenoxymethyl)chroman-4-one (prepared as described in Preparation 53), 1 ml of acetic anhydride and 10 ml of pyridine was allowed to stand for 1 day at room temperature. The reaction mixture was then poured into ice-water, stirred for 2 hours and extracted with benzene. The benzene extract was washed with 3N aqueous hydrochloric acid, water, a saturated aqueous solution of sodium bicarbonate and water in that order, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was recrystallized from a mixture of benzene and ethyl acetate (about 10:1 by volume) to give the title compound, melting at 82°-84° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104888
Source datasetuspto-grants-1992_04
ORD IDord-75984e321e7948b8922285215dbe8da0
Source noteuspto-grants-1992_04