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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 8-Acetyl-6-bromo-2,2,4,4-tetramethyl chroman | HCID 21107239 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 8-Acetoxy-6-bromo-2,2,4,4-tetramethyl chroman | HCID 57424215 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468391B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-9f21925dd17e44a9acc40f1194f99d1a |
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| Source note | uspto-grants-2008_12 |
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