HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905980Generated: October 30, 2026
1-(Trifluoromethyl)cyclopropane-1-carboxylic acid → 1-(Trifluoromethyl)cyclopropanemethanol
https://huagongshe.com/reaction/905980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(Trifluoromethyl)cyclopropane-1-carboxylic acid | HCID 2778306 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Trifluoromethyl)cyclopropanemethanol | HCID 50990661 | 77% |
Reaction Steps
50 mL of borane dimethylsulfide 2M in THF were added dropwise at RT via an addition funnel to a solution of 1-trifluormethyl-cyclopropanecarboxylic acid (10 g, 64.90 mmol) in 100 mL of THF. The resulting clear solution was stirred at 40° C. for 24 hours before being cooled to 0° C. and quenched by slow addition of aqueous saturated NH4Cl. The biphasic slurry was filtered through celite. The organic layer was separated, and the aqueous layer was back extracted twice with AcOEt. The combined organic layers were dried (Na2SO4), filtered, and evaporated to give 7 g of (1-trifluoromethyl-cyclopropyl)-methanol (77% yield). Used as in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012974B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-71db62423b974cf1b979e42b2a743845 |
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| Source note | uspto-grants-2011_09 |
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