HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018804Generated: October 31, 2026
Chlorine → 1-[3-Chloro-4-(3,3,5,5-tetramethylcyclohexyl)phenyl]ethanone
https://huagongshe.com/reaction/1018804
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 1-[4-(3,3,5,5-Tetramethylcyclohexyl)phenyl]ethanone | HCID 22390428 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[3-Chloro-4-(3,3,5,5-tetramethylcyclohexyl)phenyl]ethanone | HCID 22390425 | 74% |
Reaction Steps
40.25 g of aluminium chloride are added at 0° C., under an inert atmosphere, to 350 ml of dichloromethane, followed by addition of 5 g of 1-[4-(3,3,5,5-tetramethylcyclohexyl)phenyl]ethanone (compound V.1) dissolved in dichloromethane. After stirring for 2 hours at 0° C., 17.1 ml of chlorine gas (d=1.565, measured in the liquid state at −78° C.) are bubbled into the reaction. After warming to room temperature, a water/ice mixture is added to the reaction mixture. The resulting mixture is extracted with dichloromethane, the phases are separated after settling has taken place, and the organic phase is dried over magnesium sulphate and concentrated under reduced pressure. The residue is purified on a column of silica gel, eluting with a 7/3 (v/v) cyclohexane/dichloromethane mixutre; yield=74%; m.p.=64° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482986B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-8d60e7d78c004558bd93730df4572b87 |
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| Source note | uspto-grants-2002_11 |
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