HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231609Generated: October 25, 2026
Dichloromethane → 2-t-Butyl-4-(5-hexynoyl)-6-methylphenol
https://huagongshe.com/reaction/231609
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-tert-Butyl-6-methylphenol | HCID 16678 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | Hex-5-ynoyl chloride | HCID 2759284 | — |
| Product | 2-t-Butyl-4-(5-hexynoyl)-6-methylphenol | HCID 14672032 | 51.4% |
Reaction Steps
To a solution of 2-tert-butyl-6-methylphenol (1.2 g, 7.3 mmol) in methylene chloride (28 ml, 1.1 equiv.), stirred under argon at -78° C., is added 5-hexynoyl chloride (1.0 g) followed by tin tetrachloride (0.93 mL, 1.1 equiv.). After stirring 30 minutes at -78° C., the reaction is warmed to -50° C. and stirred 5 minutes more. The mixture is then quenched with 1N HCl/ether. The product is extracted from 1N HCl with 3 portions of ether, and the ether layers are combined and washed with water. The resulting ether layer is dried (MgSO4), filtered, and concentrated in vacuo to give 2.14 g crude product. The product is flash chromatographed on silica gel using 10% EtOAc in hexane to give 0.97 g 2-t-butyl-4-(5-hexynoyl)-6-methylphenol. Crystallization from hexane gives crystals, mp 63°-64° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04847303 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-97253f98aac7407fa153e1b9d13dad5b |
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| Source note | uspto-grants-1989_07 |
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