HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354966Generated: October 30, 2026
Isopropanol → 4-Chloro-alpha-(2-fluorophenyl)benzenemethanol
https://huagongshe.com/reaction/354966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (4-Chlorophenyl)(2-fluorophenyl)methanone | HCID 43160405 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-alpha-(2-fluorophenyl)benzenemethanol | HCID 20506263 | — |
Reaction Steps
To a stirred and refluxing mixture of 23.4 parts of (4-chlorophenyl) (2-fluorophenyl)methanone in 280 parts of 2-propanol are added portionwise 3.7 parts of sodium borohydride. Upon completion, stirring is continued for 2 hours at reflux temperature (±80° C.). The reaction mixture is cooled and decomposed by the addition of water. The 2-propanol is evaporated and the residual product is extracted with trichloromethane. The extract is dried, filtered and evaporated, yielding 4-chloro-α-(2-fluorophenyl)benzenemethanol as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377578 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-12a6cb03240a438985a160118d4a5515 |
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| Source note | uspto-grants-1983_03 |
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