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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357625Generated: November 2, 2026

Sodium borohydride → HCID 68455343, compound

https://huagongshe.com/reaction/2357625

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) before sodium borohydride (268 mg, 7078 μmol) and tetrakis(triphenylphosphine)palladium(0) (102 mg, 88 μmol) were added at ambient. 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). MS (ES+): 171(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-886493d56fc444ea9026b0e69b50dec6
Source noteuspto-grants-2010_07