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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521335Generated: October 31, 2026

Sodium borohydride → HCID 11461534, compound

https://huagongshe.com/reaction/521335

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 numberUS09328091B2
Source datasetuspto-grants-2016_05
ORD IDord-dde20869caa04610881206ff1d16c836
Source noteuspto-grants-2016_05