Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657372Generated: October 26, 2026

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

https://huagongshe.com/reaction/657372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Reactant[(3-Bromophenyl)methyl](triphenyl)phosphanium bromideHCID 19034144—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(3-bromobenzylidene)piperidine-1-carboxylateHCID 5781340928.6%

Reaction Steps

To [(3-bromophenyl)methyl](triphenyl)phosphonium bromide (1.13 mg, 2.2 mmol) in DMF (4 mL) was added NaH (52.8 mg, 2.2 mmol). This mixture was stirred at RT for 5 min, then 1,1-dimethylethyl 4-oxo-1-piperidinecarboxylate (400 mg, 2.0 mmol) was added and the pot stirred at RT for 1 h. The resultant mixture was diluted with Et2O (25 mL), washed with H2O (12+2×8 mL), brine (8 mL), dried over NaSO4, and filtered. The mixture was concentrated and purified with CombiFlash chromatograph to afford the title compound (0.2014 g, 28%). LC-MS m/z 352 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071588B2
Source datasetuspto-grants-2011_12
ORD IDord-918e641c354b4c15bf258abf5c75bc24
Source noteuspto-grants-2011_12