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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696792Generated: October 26, 2026

Hexane → tert-Butyl 3-ethynylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1696792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactanttert-Butyl 3-(2,2-dibromovinyl)piperidine-1-carboxylateHCID 86615128—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 3-ethynylpiperidine-1-carboxylateHCID 2196385593%

Reaction Steps

To a solution of 3-(2,2-Dibromo-vinyl)-piperidine-1-carboxylic acid tert-butyl ester (0.15 g, 0.42 mmol) in THF (1 ml) wad added at −78° C., 0.5 ml of n-BuLi 2.5 M in hexane (1.23 mmol). After 1 h at −78° C., the reaction mixture was quenched with 1 ml of water and the aqueous phase was extracted with AcOEt. The combined organic phase was dried over K2CO3, filtered and evaporated to give 80 mg (93%) of 3-Ethynyl-piperidine-1-carboxylic acid tert-butyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163775B2
Source datasetuspto-grants-2012_04
ORD IDord-fdfff796e719446c9c6442be03098baf
Source noteuspto-grants-2012_04