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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457581Generated: October 31, 2026

Acetic Anhydride → HCID 53799089, compound

https://huagongshe.com/reaction/1457581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 10001617HCID 10001617—
SolventDichloromethaneHCID 6344—
ProductHCID 53799089HCID 53799089—

Reaction Steps

A mixture of 4.00 g of 2-(3-cyclohexyl-3-phenylmethylureido)-4-methoxy-6-tert-butylphenol, 2.0 ml of acetic anhydride, 3.2 ml of triethylamine and 80 ml of dichloromethane was stirred at room temperature for 24 hours. The reaction mixture was washed and dried, and the solvent was removed under reduced pressure. The residue was applied to silica gel column chromatography (solvent; chloroform:ethyl acetate=9:1) to give 735 mg of O-acetyl-2-(3-cyclohexyl-3-phenylmethylureido)-4-methoxy-6-tert-butylphenol (Rf=0.75, melting point: 129°-132° C. (recrystallized from hexane)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849732
Source datasetuspto-grants-1998_12
ORD IDord-4f071abbb0be42209a0160ed1ce82950
Source noteuspto-grants-1998_12