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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816709Generated: October 31, 2026

1,6-Dibromohexane → HCID 22494777, compound

https://huagongshe.com/reaction/1816709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,6-DibromohexaneHCID 12368—
Reactanttert-Butyl 4-(acetylthio)piperidine-1-carboxylateHCID 22494773—
ReactantSodium methanolate methanolHCID 23694274—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22494777HCID 2249477761.4%

Reaction Steps

To a solution of N-t-butyloxycarbonyl-4-acetylthiopiperidine (5.5 g) in a mixture of THF (50 ml) and methanol (50 ml) was added 28% sodium methoxide methanol solution (4.76 ml) with stirring under ice-cooling and stirred at the same temperature for 30 minutes. To the solution was added 1,6-dibromohexane (17.1 g) under ice-cooling, and the mixture was successively stirred at ambient temperature for 30 minutes and then stirred at 45° C. for 2 hours. The reaction mixture was concentrated in vacuo. The resulting residue was chromatographed on silica gel (500 ml) eluting with a mixture of n-hexane and ethyl acetate (6:1 v/v). The fractions containing the desired compound were collected and evaporated under reduced pressure to give 4-(6-bromohexylthio)-N-t-butyloxycarbonylpiperidine (4.95 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884868B1
Source datasetuspto-grants-2005_04
ORD IDord-3c31a3570e304b03ac9034aa2b60d7a3
Source noteuspto-grants-2005_04