HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544813Generated: October 28, 2026
Benzoyl chloride → HCID 67201259, compound
https://huagongshe.com/reaction/544813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclohexane ethylacetate | HCID 21867204 | — |
| Reactant | 1-(2-Hydroxy-5,5-dimethylcyclohexyl)pent-4-en-1-one | HCID 67201493 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67201259 | HCID 67201259 | 28.4% |
Reaction Steps
Benzoyl chloride (12.8 g, 91 mmoles) was added dropwise to a stirred solution of 1-(2-hydroxy-5,5-dimethyl-1-cyclohexyl)-4-penten-1-one (16 g, 75 mmoles), Et3N (10 g, 99 mmoles) and DMAP (1.8 g, 15 mmoles) in CH2Cl2 (380 ml) at 20° C. and under nitrogen. The solution was heated at 45° C. during 22 hours, cooled to room temperature and washed successively with 5% aqueous HCl, 10% aqueous Na2CO3, and again with water. The organic phase was dried over Na2SO4 and concentrated to afford a brown oil. Chromatography (SiO2, AcOEt/Cyclohexane 1:9) and afforded 6.7 g of the title compound (yield=28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935669B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-b23b071b319f4df2a067183d468ea3a9 |
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| Source note | uspto-grants-2011_05 |
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