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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254192Generated: October 26, 2026

Sodium borohydride → HCID 59382996, compound

https://huagongshe.com/reaction/1254192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantTert-butyl 3-benzoyl-3-methylpiperidine-1-carboxylateHCID 59382824—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 59382996HCID 5938299671%

Reaction Steps

tert-Butyl 3-benzoyl-3-methylpiperidine-1-carboxylate (278 mg, 0.92 mmol) was dissolved in 1:1 THF/MeOH (8 mL) and NaBH4 (70 mg, 1.84 mmol, 2 equiv) was added. After stirring 30 min at rt, LC-MS showed the reaction was complete. After concentration, the residue was partitioned between ether and diluted (˜1%) aq HCl. The aqueous layer was separated and extracted twice with ether. The combined organic layers were washed with satd aq NaHCO3, brine, dried over Na2SO4 and evaporated to afford crude product which was purified by chromatography on a 12-g prepacked silica gel cartridge eluted with a 0-35% EtOAc in hexanes gradient to afford tert-butyl 3-(hydroxy(phenyl)methyl)-3-methylpiperidine-1-carboxylate (198 mg, 71%). LC-MS (3 min) tR=1.83 min, m/z 328 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455521B2
Source datasetuspto-grants-2013_06
ORD IDord-1dbcc209315142a496249478be9ebd08
Source noteuspto-grants-2013_06