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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291016Generated: October 26, 2026

Triethylamine → t-butyl [N-benzyloxycarbonyl-4-piperidinyloxy]acetate

https://huagongshe.com/reaction/1291016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl (piperidin-4-yloxy)-acetateHCID 10036224—
SolventDichloromethaneHCID 6344—
Productt-butyl [N-benzyloxycarbonyl-4-piperidinyloxy]acetateHCID 10066408495.6%

Reaction Steps

t-Butyl 4-piperidinyloxyacetate (521 mg, 2.42 mmol) and triethylamine (0.40 ml, 2.9 mmol) were dissolved in methylene chloride (20 ml) and benzyloxycarbonyl chloride (0.41 mmol, 2.9 mmol) was added. The mixture was stirred at room temperature for 74 hours. A saturated aqueous sodium hydrogencarbonate solution (50 ml) was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. After filtration, low boiling matters were distilled away from the filtrate under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=2/1). to give 710 mg of t-butyl [N-benzyloxycarbonyl-4-piperidinyloxy]acetate as a colorless oil (84%). Methylene chloride (30 ml) and trifluoroacetic acid (10 ml) were added to this oil (692 mg, 1.99 mmol) and the mixture was stirred at room temperature for 17 hours. Low boiling matters were distilled away from the reaction mixture under reduced pressure to give 555 mg of [N-benzyloxycarbonyl-4-piperidinyloxy]acetate as a colorless solid (96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753670
Source datasetuspto-grants-1998_05
ORD IDord-57e15342930f46288d49b92cff576375
Source noteuspto-grants-1998_05