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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47307Generated: October 25, 2026

Bromide ion → Benzyl 4-methylidenepiperidine-1-carboxylate

https://huagongshe.com/reaction/47307

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 numberUS06699870B2
Source datasetuspto-grants-2004_03
ORD IDord-28f15de1c3324835b374d20f7606c6c9
Source noteuspto-grants-2004_03