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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538451Generated: October 26, 2026

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

https://huagongshe.com/reaction/538451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductTert-butyl 4-(4-bromobenzyl)-4-hydroxypiperidine-1-carboxylateHCID 7085143740.4%

Reaction Steps

To a suspension of magnesium (2.9 g) in diethyl ether (50 mL) was added dropwise 1,2-dibromoethane (0.90 mL) at room temperature, and the reaction mixture was vigorously stirred at room temperature for 20 min. To the reaction mixture was added dropwise a solution of 4-bromobenzyl bromide (25 g) in diethyl ether (150 mL) over 30 min or more at 0° C., and then added dropwise a solution of tert-butyl 4-oxopiperidine-1-carboxylate (16 g) in diethyl ether (200 mL) over 30 min or more 0° C. The reaction mixture was allowed to warm to room temperature, and stirred at room temperature for 3 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution (200 mL), and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865717B2
Source datasetuspto-grants-2014_10
ORD IDord-24880964c55a49b5bcb5614bea537266
Source noteuspto-grants-2014_10