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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39742Generated: October 28, 2026

Ethanol → Tert-butyl 3-fluoro-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/39742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantTERT-BUTYL 3-FLUORO-4-OXOPIPERIDINE-1-CARBOXYLATEHCID 10560711—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 3-fluoro-4-hydroxypiperidine-1-carboxylateHCID 42609254—

Reaction Steps

To 6.5 mL of an ethanol solution containing 0.49 g of tert-butyl 3-fluoro-4-oxopiperidine-1-carboxylate, 94 mg of sodium borohydride was added under cooling with ice, and the mixture was stirred for 1 hour. The reaction mixture was added with water and ethyl acetate. The organic layer was separated, washed with an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 0.42 g of a colorless oily substance, tert-butyl 3-fluoro-4-hydroxypiperidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524738B2
Source datasetuspto-grants-2013_09
ORD IDord-f3110b9f28a34150b9b0fc30bd897fd6
Source noteuspto-grants-2013_09