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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355413Generated: October 29, 2026

Sodium borohydride → (R)-tert-butyl 3-((3-chloro-2-fluorophenyl)(hydroxy)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2355413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(R)-tert-butyl 3-(3-chloro-2-fluorobenzoyl)piperidine-1-carboxylateHCID 59382847—
SolventMethanolHCID 887—
Product(R)-tert-butyl 3-((3-chloro-2-fluorophenyl)(hydroxy)methyl)piperidine-1-carboxylateHCID 5938306356%

Reaction Steps

To a solution of (R)-tert-butyl 3-(3-chloro-2-fluorobenzoyl)piperidine-1-carboxylate (7.75 g, 22.7 mmol) in MeOH (160 mL) was added NaBH4 (6.9 g, 182 mmol) in portions such that the temperature remained below 40° C. After addition, the mixture was stirred at rt for 3 h. TLC showed the start material had disappeared. The solvent was removed in vacuo and the residue was partitioned between water and EtOAc. The organic layer was washed with H2O and brine, dried over Na2SO4 and evaporated to give (R)-tert-butyl 3-((3-chloro-2-fluorophenyl)(hydroxy)methyl)piperidine-1-carboxylate (4.35 g, 56%) which was used in the next step without purification. MS (E/Z): 344 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-de28f43b87074b0f84ad425ab443214f
Source noteuspto-grants-2010_07