HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889033Generated: October 30, 2026
Sodium borohydride → HCID 19434450, compound
https://huagongshe.com/reaction/889033
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Oxo-1-(3-trifluoromethyl-phenyl)-pyrrolidine-3-carboxylic acid ethyl ester | HCID 57429662 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19434450 | HCID 19434450 | 43% |
Reaction Steps
A mixture of 2-oxo-1-(3-trifluoromethyl-phenyl)-pyrrolidine-3-carboxylic acid ethyl ester obtained in step 2 (0.5 g, 1.6 mmol) and ethanol were cooled to 10-15° C. Sodium borohydride (0.126 g, 3.3 mmol) was added portion wise over a period of 20 min and the reaction mixture was stirred for 3.5 hrs at 20-25° C. The organic volatiles were evaporated and the residue was taken into brine solution (15 ml). The aqueous layer was extracted with ethyl acetate, dried over Na2SO4 and evaporated to obtain brown semi solid which was purified by preparative TLC to afford 3-Hydroxymethyl-1-(3-trifluoromethyl-phenyl)-pyrrolidin-2-one as a colorless oil (0.177 g, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252797B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-5ff374fc80a8489eb5aaf95d754e862a |
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| Source note | uspto-grants-2012_08 |
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