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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881024Generated: October 29, 2026

Sodium Chloride → tert-Butyl 4-(3-bromopropyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/881024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl 4-(3-hydroxypropyl)tetrahydro-1(2h)-pyridinecarboxylateHCID 2800739—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(3-bromopropyl)piperidine-1-carboxylateHCID 1840908198%

Reaction Steps

To a tetrahydrofuran (110 mL) solution of 10.7 g of tert-butyl 4-(3-hydroxypropyl)-1-piperidinecarboxylate was added 19.0 g of carbon tetrabromide under cooling with water, to which 15.0 g of triphenylphosphine was then added over a period of 13 minutes. This mixture was stirred at room temperature for 2 hours and 30 minutes and allowed to stand for 13 hours. To the reaction mixture were added water, ethyl acetate, and a saturated sodium chloride aqueous solution. The organic layer was separated, washed with a saturated sodium chloride aqueous solution, and dried with anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The resultant residue was purified using silica gel column chromatography (eluent; hexane:ethyl acetate=3:1) to provide 13.2 g of tert-butyl 4-(3-bromopropyl)-1-piperidinecarboxylate as colorless oily form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993603B2
Source datasetuspto-grants-2015_03
ORD IDord-e13abaa26faa4db3bcea077b5cd40093
Source noteuspto-grants-2015_03