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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396318Generated: October 29, 2026

Sodium borohydride → 1-Benzyl-4-hydroxy-3-isopropylpiperidine

https://huagongshe.com/reaction/396318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23003699HCID 23003699—
SolventMethanolHCID 887—
Product1-Benzyl-4-hydroxy-3-isopropylpiperidineHCID 23003711—

Reaction Steps

Sodium borohydride (0.5 g, 15.6 mmole) was added to the stirred solution of 1-benzyl-3-isopropylpiperid-4-one (3.3 g, 14.2 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-isopropylpiperidine as oil. Yield 2.9 g (85%), C15H23NO, m/z 234 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608078B2
Source datasetuspto-grants-2003_08
ORD IDord-6333fe5c6c9942e694edddd51596d8da
Source noteuspto-grants-2003_08