Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531463Generated: October 25, 2026

Sodium hydride → Tert-butyl 4-(3-bromobenzylidene)piperidine-1-carboxylate

https://huagongshe.com/reaction/531463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTriethyl phosphiteHCID 31215—
Reactant3-Bromobenzyl bromideHCID 69979—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductTert-butyl 4-(3-bromobenzylidene)piperidine-1-carboxylateHCID 5781340951.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

The mixture of 1-bromo-3-(bromomethyl)benzene (6.2 g, 24.8 mmol) and triethyl phosphite (4.53 g, 27.28 mmol) was heated at 90° C. for 12 hours, cooled to 0° C., added DME (40 ml) and tert-butyl 4-oxopiperidine-1-carboxylate (5.73 g, 28.8 mmol) and sodium hydride (1.19 g, 49.6 mmol) and stirred at RT for 2-3 hours. Diluted with water and extracted with ether to afford 4.5 g (51.5% yield) of the titled product after purification with (60/120 silica gel) column chromatography using 10% ethyl acetate in hexane as eluent. MS: m/z=353.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353107B2
Source datasetuspto-grants-2016_05
ORD IDord-7449a3134678448683907a8a825d8072
Source noteuspto-grants-2016_05