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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584218Generated: November 1, 2026

Triethylamine → 1-(Benzyloxycarbonyl)-3-(2,3-dimethoxybenzyl)piperazine

https://huagongshe.com/reaction/584218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22342949HCID 22342949—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(Benzyloxycarbonyl)-3-(2,3-dimethoxybenzyl)piperazineHCID 2234271053.1%

Reaction Steps

A solution of benzyloxycarbonyl chloride (0.59 g) in dichloromethane (3.0 ml) was added dropwise to a solution of 2-(2,3-dimethoxybenzyl)piperazine (0.91 g) and triethylamine (0.64 ml) in dichloromethane (18 ml) below 5° C. over 5 minutes under ice-cooling, and the reaction mixture was stirred at the same temperature for 15 minutes. After 2 hours of stirring at room temperature, the mixture was poured into a mixed solvent of water (40 ml) and dichloromethane (25 ml) and the whole was adjusted to pH 9 with aqueous sodium hydrogen carbonate solution. The organic layer was separated, washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (20 g) using a mixed solvent of dichloromethane and methanol (40:1). The fractions containing the objective compound were collected and evaporated under reduced pressure to give colorless oil of 1-(benzyloxycarbonyl)-3-(2,3-dimethoxybenzyl)piperazine (0.68 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924278B2
Source datasetuspto-grants-2005_08
ORD IDord-328a69c68dc94231a7094a2e031bd54d
Source noteuspto-grants-2005_08