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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218390Generated: October 31, 2026

Sodium borohydride → HCID 58011549, compound

https://huagongshe.com/reaction/218390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58011496HCID 58011496—
SolventMethanolHCID 887—
ProductHCID 58011549HCID 5801154941%

Reaction Steps

To a solution of (R)-tert-butyl 3-((R)-(2-ethoxy-2-oxoethoxy)(3-fluorophenyl)methyl)piperidine-1-carboxylate (29.88 g, 75.9 mmol) in MeOH (300 mL) was added NaBH4 (23 g, 605.2 mmol) in portions while the temperature was lower than 40° C. After addition, the mixture was stirred at rt for 2-3 hr. The solvent was removed in vacuo to give a residue which was partitioned between water and EtOAc. The organic layer was washed with H2O and brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified on silica gel chromatography to afford (R)-tert-butyl 3-((R)-(3-fluorophenyl)(2-hydroxyethoxy)methyl)piperidine-1-carboxylate (11 g, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198453B2
Source datasetuspto-grants-2012_06
ORD IDord-b71db5fc1b65413ca87024305fe65529
Source noteuspto-grants-2012_06