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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451703Generated: October 30, 2026

Sodium borohydride → HCID 59201356, compound

https://huagongshe.com/reaction/451703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59201712HCID 59201712—
SolventMethanolHCID 887—
ProductHCID 59201356HCID 5920135642.9%

Reaction Steps

To a solution of (R)-tert-butyl 3-(3-fluoro-5-methylbenzoyl)piperidine-1-carboxylate (1.7 g, 5.3 mmol) in MeOH (30 mL), NaBH4 (1.61 g, 42.3 mmol) was added in portions and stirred overnight. The reaction was quenched with the addition of water (50 mL) and evaporated in vacuo until MeOH was removed. The aqueous layer was extracted with EA, washed with brine and dried over Na2SO4. The crude product was purified by chromatography to give (R)-tert-butyl 3-((R)-(3-fluoro-5-methylphenyl)(hydroxy)methyl)piperidine-1-carboxylate (730 mg, 42.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487108B2
Source datasetuspto-grants-2013_07
ORD IDord-c0a6e4c00a8549fdb5a7f17e308dbf5f
Source noteuspto-grants-2013_07