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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357609Generated: November 2, 2026

Sodium borohydride → HCID 68455343, compound

https://huagongshe.com/reaction/2357609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86607614HCID 86607614—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
ProductHCID 68455343HCID 68455343—

Reaction Conditions

Temperature50 °C

Reaction Steps

(R)-Allyl 2-(isopropylcarbamoyl)-5-methylpyrrolidine-1-carboxylate (450 mg, 1769 μmol) was dissolved in acetonitrile (13 mL) and sodium borohydride (268 mg, 7078 μmol) and tetrakis(triphenylphosphine)palladium(0)(102 mg, 88 μmol) were added at ambient temperature. The reaction mixture was heated to 50° C. for 4 h, then filtered through a pad of silica gel and washed with chloroform to remove impurities. The silica was washed again with methanol to obtain the title compound as a mixture of diastereomers (˜60:40). Found MS (ES+): 171(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-7085ea27014f4d6abd0979f4159a7a4e
Source noteuspto-grants-2010_07