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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300145Generated: October 31, 2026

Pyridine, hydrofluoride (1:1) → Benzyl 4-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2300145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine, hydrofluoride (1:1)HCID 64774—
ReactantSodium BicarbonateHCID 516892—
ReactantBenzyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 13016598—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-fluoro-4-(hydroxymethyl)piperidine-1-carboxylateHCID 22135584—

Reaction Steps

A mixture of 5 ml hydrogen fluoride pyridine and 20 ml methylene chloride was cooled, and 10 ml solution of 4.95 g of benzyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate in methylene chloride was added dropwise thereinto over 25 min such that the bulk temperature was 0° C. or less. The mixture was stirred for 35 min under ice-cooling. The reaction solution was poured into a mixture of saturated sodium bicarbonate and ice. The organic layer was recovered, dried over anhydrous magnesium sulfate, and filtered. The filtrate was evaporated, and then subjected to silica gel column chromatography to give 2.84 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498159B1
Source datasetuspto-grants-2002_12
ORD IDord-c8fcbd16c4f94cdcb57e9f9718a69561
Source noteuspto-grants-2002_12