Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340095Generated: October 30, 2026

Sodium borohydride → HCID 11461534, compound

https://huagongshe.com/reaction/340095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl 4-(4-chlorobenzoyl)piperidine-1-carboxylateHCID 10519988—
SolventEthanolHCID 702—
ProductHCID 11461534HCID 1146153494.8%

Reaction Steps

tert-Butyl 4-(4-chlorobenzoyl)piperidine-1-carboxylate (3.63 g, 11.2 mmol) was dissolved in ethanol (100 mL) then sodium tetrahydroborate (424 mg, 112 mmol) was added to this solution. The reaction mixture was stirred at room temperature for 3 h. LC-MS analysis of the reaction mixture showed no more starting material. The crude reaction mixture was concentrated and the residue was diluted with EtOAc (100 mL) and washed with water (2×50 mL) and brine (50 mL). The organic layer was dried over Na2SO4, filtered and concentrated to yield tert-butyl 4-((4-chlorophenyl)(hydroxy)methyl)piperidine-1-carboxylate (3.46 g, 94%), which was used in the next step directly. m/z: 326 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895566B2
Source datasetuspto-grants-2014_11
ORD IDord-2ee60e5b8b654cbe9fc4d5216702dcee
Source noteuspto-grants-2014_11