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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223735Generated: October 30, 2026

Diethyl Ether → 4-Benzyl-1-(2-benzyloxycarbonylamino-ethyl)-piperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2223735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDiisopropylethylamineHCID 81531—
Reactantbenzyl N-(2-bromoethyl)carbamateHCID 278694—
ReactantEthyl 4-benzylpiperidine-4-carboxylateHCID 53297794—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyl-1-(2-benzyloxycarbonylamino-ethyl)-piperidine-4-carboxylic acid ethyl esterHCID 59715929—

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Benzyl-piperidine-4-carboxylic acid ethyl ester (2.5 g, 10 mmol), (2-bromo-ethyl)-carbamic acid benzyl ester (2.58 g, 10 mmol) and DIPEA (1.7 mL, 10 mmol) are dissolved in THF (50 mL) and heated at 80° C. for 15 h. The mixture is poured into Et2O (200 mL) and washed with sat. Na2CO3 (50 mL). The ether phase is extracted with 1M aqueous HCl (3×50 mL), the aqueous extracts washed with ether (50 mL) and adjusted to pH 14 with cooled 33% aqueous NaOH. The aqueous phase is extracted with CH2Cl2 (4×50 mL). The organic extracts are dried (Na2SO4), filtered and evaporated to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375227B2
Source datasetuspto-grants-2008_05
ORD IDord-6321cd404e1d42c98e78b5a8598096aa
Source noteuspto-grants-2008_05