HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404895Generated: October 31, 2026
Lithium borohydride → HCID 59410112, compound
https://huagongshe.com/reaction/2404895
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 59410118 | HCID 59410118 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59410112 | HCID 59410112 | — |
Reaction Steps
To a suspension of LiBH4 (55 mg, 2.54 mmol) in anhydrous THF (3 mL) was added a solution of (S)-methyl 4,4-difluoro-1-(4-nitro-3-(trifluoromethyl)phenyl)pyrrolidine-2-carboxylate (300 mg, 0.85 mmol) in anhydrous THF at 0° C. The reaction mixture was stirred at 0° C. for 20 min then allowed to come to room temperature and stirred overnight. The reaction mixture was diluted with ethyl acetate (100 mL), washed with water (50 mL), and then brine. The layers were separated, and the organic layer was dried over Na2SO4, filtered, and concentrated to afford (S)-(4,4-difluoro-1-(4-nitro-3-(trifluoromethyl)phenyl)pyrrolidin-2-yl)methanol as a yellow, viscous oil (275 mg, 100%). LC/MS: m/z 327.2 (M+H)+ at 1.54 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802700B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-40fdb9e00687492287c3f6fd6890bb87 |
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| Source note | uspto-grants-2014_08 |
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