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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637374Generated: November 1, 2026

Sodium borohydride → HCID 57248109, compound

https://huagongshe.com/reaction/1637374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(2R,5R)-2-(t-butyl)-5-[(1S)-3-oxocyclopentyl]-5-phenyl-1,3-dioxolan-4-oneHCID 54308542—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 57248109HCID 57248109118.9%

Reaction Steps

To a solution of 169 mg of (2R,5R)-2-(t-butyl)-5-[(1S)-3-oxocyclopentyl]-5-phenyl-1,3-dioxolan-4-one in 2 ml of methanol, 71 mg of sodium borohydride was added under cooling with ice, followed by stirring for 30 minutes at the same temperature. The reaction mixture was diluted with diethyl ether, washed with water and then brine, and dried over anhydrous magnesium sulfate. Distilling the solvent off under reduced pressure, 157 mg of the title compound was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040449
Source datasetuspto-grants-2000_03
ORD IDord-f4eb51a699e24f30993fcb85e06b68f0
Source noteuspto-grants-2000_03