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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8744Generated: October 25, 2026

1-Pentene, 5-bromo- → Methyl 4-(pent-4-en-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/8744

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Pentene, 5-bromo-HCID 70704—
Reactant1-N-Boc-4-Piperidinecarboxylic acid methyl esterHCID 392870—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(pent-4-en-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylateHCID 1123218199.2%

Reaction Steps

To a solution of potassium bis(trimethylsilyl)amide (30.7 g, 0.15 mol) in tetrahydrofuran (750 mL) at 0° C. was added a solution of methyl 1-(tert-butoxycarbonyl)piperidine-4-carboxylate (25 g, 0.10 mol) from Step A in tetrahydrofuran (250 mL) and the reaction mixture was stirred for 1 h. 5-Bromo-1-pentene (19.4 mL, 0.164 mol) was added and the reaction mixture was allowed to warm to room temperature for 1.5 h. The reaction mixture was then poured into saturated sodium bicarbonate solution and extracted three times with ethyl acetate. The organic layers were combined and washed with brine, dried over sodium sulfate, filtered, and concentrated to afford the title compound (30.9 g) which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091211B2
Source datasetuspto-grants-2006_08
ORD IDord-292d55b0aa854c219dbd269febe9a838
Source noteuspto-grants-2006_08