HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276540Generated: October 30, 2026
Acetyl chloride → 1-(1,2,3,5,6,7-Hexahydro-s-indacen-4-yl)ethanone
https://huagongshe.com/reaction/1276540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1,2,3,5,6,7-Hexahydro-s-indacene | HCID 136321 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(1,2,3,5,6,7-Hexahydro-s-indacen-4-yl)ethanone | HCID 382669 | — |
Reaction Steps
To a stirred solution of 1,2,3,5,6,7-Hexahydro-s-indacene (30 grams) and acetyl chloride (14.2 mL) in 120 mL of benzene at 0° C. was added 30 grams of aluminum chloride over a period of 1 hour. The cooling bath was removed and the solution was warmed to room temperature and stirred for 4 hours. The deep red mixture was then poured onto a mixture of 270 grams of ice and 50 mL of concentrated hydrochloric acid. The layers were separated and the aqueous phase was extracted with diethyl ether. The combined organic phases were washed with saturated sodium bicarbonate solution and brine, dried over anhydrous sodium sulfate and concentrated in vacuo to afford an orange solid which was recrystallized from hexane to give 34 grams of the title compound, m.p. 69.1-76.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06166064 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-54214663314b4574aadeed09f237f83b |
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| Source note | uspto-grants-2000_12 |
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