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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303622Generated: November 2, 2026

Tert-butyl 4-(3,3-dibromoallyl)piperidine-1-carboxylate → Tert-butyl 4-(prop-2-yn-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2303622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(3,3-dibromoallyl)piperidine-1-carboxylateHCID 15503387—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(prop-2-yn-1-yl)piperidine-1-carboxylateHCID 1818754679.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 118 mg (0.31 mmol) of 1-(t-butoxycarbonyl)-4-(3,3-dibromoprop-2-en-1-yl)piperidine from Step A in THF (4 mL) at −78° C. was added a 2.5M solution of n-butyl lithium (0.370 mL, 0.92 mmol). After stirring at −78° C. for 45 min, the reaction mixture was quenched with sat'd ammonium chloride (4 mL) and diluted with ether (25 mL). After separating the phases, the aqueous layer was extracted with ether. The combined organic phases were washed with brine, dried over magnesium sulfate and concentrated. The residue was purified by FC (4:1 v/v hexanes/ether) to give the title compound (55 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432981B1
Source datasetuspto-grants-2002_08
ORD IDord-e480245a1ddf418c94c8ff6a5ba50cf7
Source noteuspto-grants-2002_08