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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396338Generated: October 29, 2026

Sodium borohydride → HCID 23003647, compound

https://huagongshe.com/reaction/396338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3,5-Diethyl-3-methyl-1-(phenylmethyl)-4-piperidinoneHCID 22278878—
SolventMethanolHCID 887—
ProductHCID 23003647HCID 23003647—

Reaction Steps

Sodium borohydride (0.18 g, 4.8 mmole) was added to the stirred solution of 1-benzyl-3,5-diethyl-3-methylpiperidin-4-one (2.0 g, 7.72 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-3,5-diethyl-4-hydroxy-3-methylpiperidine as oil. Yield 1.8 g (89%), C17H27NO, m/z 262 (M+l).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608078B2
Source datasetuspto-grants-2003_08
ORD IDord-c82c1ff15c98495c9ae641759fe7f02d
Source noteuspto-grants-2003_08