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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240390Generated: October 30, 2026

1,2-Dibromoethane → Tert-butyl 4-(4-fluorobenzyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/240390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
Reactant4-Fluorobenzyl chlorideHCID 9602—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(4-fluorobenzyl)-4-hydroxypiperidine-1-carboxylateHCID 23526831—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a suspension of magnesium (1.2 g) and 1,2-dibromoethane (0.11 mL) in THF (30 mL) was added a solution of 4-fluorobenzyl chloride (6.3 mL) in THF (10 mL) at room temperature under a nitrogen atmosphere, and the mixture was stirred for 1 hr at the same temperature. The reaction mixture was 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 stirred for 2 days. To the reaction mixture was added water at 0° C., and then saturated aqueous potassium sodium tartrate solution, 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 (4.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648079B2
Source datasetuspto-grants-2014_02
ORD IDord-1985f382c63c47e48eec7d952b47fc60
Source noteuspto-grants-2014_02