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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306501Generated: October 31, 2026

1,6-Dibromohexane → HCID 18434316, compound

https://huagongshe.com/reaction/2306501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium HydroxideHCID 14798—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
ProductHCID 18434316HCID 18434316—

Reaction Steps

A mixture of 7 g of tert-butyl (4-hydroxy)-piperidine-1-carboxylate and 210 ml of 1,6-dibromohexane is treated firstly with 3.5 g of tetrabutylammonium hydrogen sulphate and then with 210 ml of 50% aqueous sodium hydroxide solution. After stirring at room temperature for 5 days the reaction mixture is diluted with methylene chloride, the organic phase is separated and the aqueous phase is extracted with methylene chloride. The combined organic phases are washed with saturated sodium chloride solution, dried and concentrated. The brown oil is chromatographed on silica gel with ethyl acetate-hexane. 10.9 g of tert-butyl 4-(6-bromo-hexyloxy)-piperidine-1-carboxylate are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441177B1
Source datasetuspto-grants-2002_08
ORD IDord-5541e5432f7f40b6976395bd9d812fc5
Source noteuspto-grants-2002_08