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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279258Generated: October 30, 2026

Sodium borohydride → HCID 66980952, compound

https://huagongshe.com/reaction/2279258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67130093HCID 67130093—
SolventEthanolHCID 702—
ProductHCID 66980952HCID 6698095269.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (R)-methyl 3-(4-cyano-3-(trifluoromethyl)phenyl)-1-methyl-2-oxoimidazolidine-4-carboxylate (25f) (0.330 g, 1.01 mmol) in EtOH (20 mL), cooled to 0° C., Sodium borohydride (0.045 g, 1.21 mmol) was added portion wise maintaining the temperature at 0° C. The reaction mixture was slowly warmed to room temperature and stirred for further 6 h. After completion (by TLC) the volatiles were removed under reduced pressure and the crude residue was extracted with EtOAc (3×20 mL). The combined organic extracts were dried over Na2SO4 and concentrated under reduced pressure to provide the crude reaction mixture which was purified by column chromatography to afford the alcohol 25g (0.21 g, 69%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133182B2
Source datasetuspto-grants-2015_09
ORD IDord-89f57289508e4157a25e1c131318e192
Source noteuspto-grants-2015_09