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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377331Generated: October 28, 2026

Dichloromethane → 8-Acetoxy-6-bromo-2,2,4,4-tetramethyl chroman

https://huagongshe.com/reaction/2377331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantEthyl AcetateHCID 8857—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant8-Acetyl-6-bromo-2,2,4,4-tetramethyl chromanHCID 21107239—
SolventHexaneHCID 8058—
Product8-Acetoxy-6-bromo-2,2,4,4-tetramethyl chromanHCID 5742421592%

Reaction Steps

A solution of 8-acetyl-6-bromo-2,2,4,4-tetramethyl chroman (Intermediate 15A, 1.3 g, 4.18 mol) in anhydrous dichloromethane (30 mol) was treated with a 77% aqueous solution of 3-chloroperoxybenzoic acid (5.75 g, 33.44 mmol) and the resulting reaction mixture was stirred at ambient temperature for 24 h. The reaction mixture was then cooled in an ice bath and cautiously quenched with saturated sodium thiosulfate solution. The phases were separated and the organic phase was washed with saturated, aqueous sodium bicarbonate solution, water and brine, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford a residue that on flash column chromatography over silica gel (230-400 mesh) using 10% ethyl acetate in hexane as the eluent afforded the title compound as an oil (1.3 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468391B2
Source datasetuspto-grants-2008_12
ORD IDord-9f21925dd17e44a9acc40f1194f99d1a
Source noteuspto-grants-2008_12