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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396320Generated: October 29, 2026

Sodium borohydride → HCID 70028630, compound

https://huagongshe.com/reaction/396320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68684462HCID 68684462—
SolventMethanolHCID 887—
ProductHCID 70028630HCID 70028630—

Reaction Steps

Sodium borohydride (0.4 g, 12.2 mmole) was added to the stirred solution of 1-benzyl-3-n-butylpiperidin-4-one (2.8 g, 9.3 mmole) in methanol (20 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-3-n-butyl-4-hydroxypiperidine as oil. Yield 2.5 g (86%), C16H25NO, m/z 248 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608078B2
Source datasetuspto-grants-2003_08
ORD IDord-a64e2511cd1e436288b5d999e27e4f69
Source noteuspto-grants-2003_08