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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396314Generated: October 30, 2026

Sodium borohydride → HCID 23003650, compound

https://huagongshe.com/reaction/396314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13016601HCID 13016601—
SolventMethanolHCID 887—
ProductHCID 23003650HCID 23003650—

Reaction Steps

Sodium borohydride (0.5 g, 15.6 mmole) was added to the stirred solution of 1-benzyl-3-n-propylpiperidin-4-one (4.0 g, 17.3 mmole) in methanol (25 ml) at 0-5° C. over a period of 5 min, and stirring was continued for 1 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water (20 ml) and extracted with ethyl acetate. The ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to furnish 1-benzyl-4-hydroxy-3-n-propylpiperidine as oil. Yield 3.3 g (81%), C15H23NO, m/z 234 (M+l).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608078B2
Source datasetuspto-grants-2003_08
ORD IDord-1554478d22304cdfbe9b5e889b39ca41
Source noteuspto-grants-2003_08