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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195674Generated: November 1, 2026

Sodium borohydride → HCID 54435245, compound

https://huagongshe.com/reaction/1195674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14011078HCID 14011078—
SolventEthanolHCID 702—
ProductHCID 54435245HCID 54435245—

Reaction Steps

Sodium borohydride (1.13 g, 30 mmol) was added to a stirred suspension of 1-benzoyl-4-(4-acetamidobenzoyl)piperidine (10.0 g, 29 mmol) in ethanol (300 ml), cooled in a water bath. The mixture was stirred at room temperature for 1 hour then additional sodium borohydride (1.13 g, 30 mmol) was added and stirring was continued for 2 hours. The solvent was evaporated under reduced pressure and water (200 ml), HCl--H2O (6M, 15 ml) and methanol (15 ml) were added. The mixture was extracted with dichloromethane (4×200 ml) and the combined organic fractions were dried (Na2SO4) and evaporated under reduced pressure to give an off-white solid which was crystallized from ethanol to give the piperidine as white crystals. (5.77 g, 57%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112824
Source datasetuspto-grants-1992_05
ORD IDord-195f5f1dc36949b5b5b1a2b1ef93d8a8
Source noteuspto-grants-1992_05