HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406032Generated: October 30, 2026
m-Chloroperbenzoic acid → 4,4-Difluorocyclohexan-1-ol
https://huagongshe.com/reaction/406032
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 1-(4,4-Difluorocyclohexyl)ethan-1-one | HCID 14365663 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4,4-Difluorocyclohexan-1-ol | HCID 546300 | — |
Reaction Steps
0.361 g meta-chloro-perbenzoic acid were added into a solution of 0.262 g 1-(4,4-difluoro-cyclohexyl)-ethanone in 5 ml chloroform. The reaction was stirred at rt for 2 hours when TLC indicated consumption of the 1-(4,4-difluoro-cyclohexyl)-ethanone. The solution was poured into saturated sodium hydrogencarbonate solution and extracted with chloroform (3×50 ml). The combined organic phases were passed through a phase separator concentrated in vacuo. The crude product was resuspended in methanol (5 ml) and 10% aq. potassium carbonate solution. (5 ml) and stirred at rt over a weekend. The solution was diluted with chloroform (25 ml) and sat. sodium hydrogencarbonate solution. The organic phases were separated and the aqueous phase was extracted with methylene chloride (3×25 ml). The combined organic phases were passed through a phase-separator, concentrated in vacuo. Purification was achieved by silica gel column chromatography (solvent: 100%→1:1 petroleum ether/diethylether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754079B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-fb29d54c051747bf9c94647271ba8dfc |
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| Source note | uspto-grants-2014_06 |
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