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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291151Generated: October 31, 2026

Triethylamine → 1-(3-Fluorobenzyl)piperidin-4-ol

https://huagongshe.com/reaction/1291151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Fluorobenzyl bromideHCID 68007—
ReactantPiperidin-4-olHCID 79341—
SolventDimethylformamideHCID 6228—
Product1-(3-Fluorobenzyl)piperidin-4-olHCID 380231844.8%

Reaction Steps

1.28 g (0.0127 mol) of 4-hydroxypiperidine were dissolved in 60 ml of dimethylformamide and cooled to 0°. 3.0 g (0.0159 mol) of 3-fluoro-benzyl bromide and 5.0 ml (0.0349 mol) of triethylamine were added under argon and the mixture was left to come to room temperature. It was stirred for 16 hrs., the solvent was distilled off and the residue was chromatographed on silica gel with dichloromethane/methanol (19:1) as the eluent. 1.19 g (36%) of 1-(3-fluoro-benzyl)-piperidin-4-ol was obtained as yellow crystals; m.p. 61°-62°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-79a5026af527465eb25f426f558e0cf3
Source noteuspto-grants-1998_05