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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539690Generated: October 25, 2026

Hydrochloric Acid → Tert-butyl 4-(3,4-difluorobenzyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/539690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,2-DibromoethaneHCID 7839—
Reactant4-(Bromomethyl)-1,2-difluorobenzeneHCID 581436—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantMagnesiumHCID 5462224—
ReactantPotassium sodium tartarateHCID 9855836—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(3,4-difluorobenzyl)-4-hydroxypiperidine-1-carboxylateHCID 8668086259.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a suspension of magnesium (1.2 g) and 1,2-dibromoethane (0.11 mL) in diethyl ether (30 mL) was added a solution of 3,4-difluorobenzyl bromide (10 g) in diethyl ether (10 mL) at room temperature under a nitrogen atmosphere, and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was diluted with THF (30 mL), and cooled to −78° C. A solution of tert-butyl 4-oxopiperidine-1-carboxylate (5.0 g) in THF (10 mL) was added thereto, and the mixture was allowed to warm to room temperature, and was stirred overnight. To the reaction mixture was added a small amount of 1N hydrochloric acid at 0° C. to quench the reaction. Saturated aqueous potassium sodium tartrate solution was added thereto, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane), and recrystallized from ethyl acetate/hexane to give the title compound (4.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871766B2
Source datasetuspto-grants-2014_10
ORD IDord-313a2d8d585047c8b67d6c06f4797822
Source noteuspto-grants-2014_10