HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185255Generated: October 29, 2026
Acetyl chloride → 8-Acetyl-6-bromo-2,2,4,4-tetramethyl chroman
https://huagongshe.com/reaction/2185255
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 6-Bromo-2,2,4,4-tetramethylchroman | HCID 12137005 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Acetyl-6-bromo-2,2,4,4-tetramethyl chroman | HCID 21107239 | 83% |
Reaction Steps
A stirred, cooled (ice bath) suspension of aluminum chloride (0.99 g, 7.46 mmol) in anhydrous dichloromethane (20 mL) was treated with acetyl chloride (0.58 g, 7.46 mmol). After 5 minutes, a solution of 6-bromo-2,2,4,4-tetramethyl chroman (1 g, 3.73 mmol)in dichloromethane was added. The reaction was allowed to warn to ambient temperature and stirred for 2 h. The reaction mixture was then poured into ice containing 10% hydrochloric acid and extracted with diethyl ether (×2). The combined organic phase was washed with saturated aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to a residue which was subjected to flash column chromatography over silica gel (230-400 mesh) using 5% ethyl acetate in hexane as the eluent to afford the title compound as a pale yellow oil (0.95 g, 83%). It was used as such for the next step without any characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399774B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-c957787f0cbb46ff919aa9c5bfe1fefd |
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| Source note | uspto-grants-2002_06 |
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