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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084648Generated: November 1, 2026

Sodium borohydride → HCID 19978935, compound

https://huagongshe.com/reaction/1084648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15754168HCID 15754168—
SolventEthanolHCID 702—
ProductHCID 19978935HCID 1997893590%

Reaction Steps

4.0 g (0.013 mol) of 1-(α,α-dimethylbenzyl)-2,4-dioxo-3-phenylpiperidine prepared by the method of Reference Example 18, was dissolved in 50 ml of ethanol, and 0.27 g (0.007 mol) of sodium- borohydride was added thereto at room temperature. The mixture was stirred at room temperature for 30 minutes, and then ethanol was distilled off under reduced pressure. Water was added to the residue, and precipitated crystals were collected by filtration. The crude product thereby obtained was recrystallized from ethanol to obtain 3.6 g (yield: 90.0%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05006157
Source datasetuspto-grants-1991_04
ORD IDord-71b1c166ef4643679c6bd1f63c62d1a8
Source noteuspto-grants-1991_04