HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198027Generated: October 26, 2026
1-Bromo-3,5-bis(trifluoromethyl)benzene → (3S)-1-[3,5-bis(trifluoromethyl)phenyl]pyrrolidin-3-ol
https://huagongshe.com/reaction/2198027
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3,5-bis(trifluoromethyl)benzene | HCID 67602 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | (S)-3-Hydroxypyrrolidine hydrochloride | HCID 22309122 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (3S)-1-[3,5-bis(trifluoromethyl)phenyl]pyrrolidin-3-ol | HCID 46941682 | 28% |
Reaction Steps
A solution of 3,5-bis(trifluoromethyl)phenyl bromide (44.0 g), (S)-3-hydroxypyrrolidine hydrochloride (17.8 g), tris(dibenzylideneacetone)dipalladium(0) (5.88 g), (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (8.00 g) and sodium tert-butoxide (36.0 g) in toluene (280 ml) was refluxed with stirring under an argon gas atmosphere for 16 hr. After cooling to room temperature, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated, and the residue was purified by silica gel column chromatography (petroleum ether:ethyl acetate 20:1-2:1) to give the title compound (12.0 g, yield 28%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338622B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-e645636b00b045c4adfdb98b6337d8c4 |
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| Source note | uspto-grants-2012_12 |
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