Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412909Generated: October 31, 2026

Water → HCID 18538905, compound

https://huagongshe.com/reaction/412909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBis(2-chloroethyl) etherHCID 8115—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-(4-aminobenzyl)piperidine-1-carboxylateHCID 21876872—
Solvent1-ButanolHCID 263—
ProductHCID 18538905HCID 1853890569.9%

Reaction Steps

1-tert-Butoxycarbonyl-4-(4-aminobenzyl)piperidine (1 g, 3.45 mmol) was dissolved in 1-butanol (20 mL). To the solution were added bis(2-chloroethyl) ether (490 mg, 3.45 mmol) and potassium carbonate (1 g, 7.23 mmol), and the mixture was heated for 30 hours under reflux. The reaction mixture was poured into water (50 mL), and the mixture was extracted with ethyl acetate. The extract was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the concentrate was purified by silica gel column chromatography (hexane/ethyl acetate=3/1) to give 1-tert-butoxycarbonyl-4-(4-morpholinobenzyl)piperidine (869 mg) as a colorless oily substance. This compound (859 mg, 2.39 mmol) was dissolved in ethyl acetate (10 mL). To the solution was added 4N-hydrogen chloride in ethyl acetate (5 mL), and the mixture was stirred at room temperature for 2 hours. The solvent was distilled off under reduced pressure to give the titled compound (562 mg) as colorless powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562978B1
Source datasetuspto-grants-2003_05
ORD IDord-7480f6d2e71442a69623d3d5866ba8ff
Source noteuspto-grants-2003_05