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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300143Generated: October 26, 2026

Bromide ion → Benzyl 4-methylidenepiperidine-1-carboxylate

https://huagongshe.com/reaction/2300143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
ReactantHCID 178418922HCID 178418922—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 4-methylidenepiperidine-1-carboxylateHCID 15519136159.7%

Reaction Steps

51.1 g of methyltoluphenylphosphonium bromide was added to a mixture of 16.1 g tert-butoxy potassium and 500 ml tetrahydrofuran, and then stirred for 1 hr and 20 min at room temperature. 16.1 g of benzyl 4-oxo-1-piperidinecarboxylate was added thereto, and the mixture was stirred for 2 hr and 40 min at room temperature. The reaction solution was evaporated, diethyl ether was added thereto, and then filtered through Celite. The filtrate was washed with water and brine, dried over anhydrous magnesium sulfate, and then filtered. The filtrate was evaporated, and the resulting residue was subjected to silica gel column chromatography to give 25.5 g of benzyl 4-methylene-1-piperidinecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498159B1
Source datasetuspto-grants-2002_12
ORD IDord-38d2746c90ab49d69f41b89142ceb2ac
Source noteuspto-grants-2002_12