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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396333Generated: October 29, 2026

Sodium borohydride → HCID 23003714, compound

https://huagongshe.com/reaction/396333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22278870HCID 22278870—
SolventMethanolHCID 887—
ProductHCID 23003714HCID 23003714—

Reaction Steps

Sodium borohydride (0.2 g, 5.26 mmole) was added to the stirred solution of 1-benzyl-3,3,5-trimethylpiperidin-4-one (2.0 g, 8.73 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-3,3,5-trimethylpiperidine as oil. Yield 1.9 g (91%), C15H23NO, m/z 234 (M+l).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608078B2
Source datasetuspto-grants-2003_08
ORD IDord-e25741db05c644f985c1042b751ef8ea
Source noteuspto-grants-2003_08