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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862660Generated: October 27, 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/1862660

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 numberUS06538002B1
Source datasetuspto-grants-2003_03
ORD IDord-dc3a3a0874a041d7ab274de3faf9a8c7
Source noteuspto-grants-2003_03