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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381190Generated: November 3, 2026

Triethylamine → o-Methoxycarbonyl--[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide

https://huagongshe.com/reaction/1381190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantVeratroyl chlorideHCID 77070—
Reactanto-Methoxycarbonyl-alpha-(1-piperazinyl)acetanilideHCID 13117362—
SolventDichloromethaneHCID 6344—
Producto-Methoxycarbonyl--[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilideHCID 13117363—

Reaction Steps

6.5 Grams of o-methoxycarbonyl-α-(1-piperazinyl)acetanilide and 2.4 g of triethylamine were dissolved in 50 ml of methylene chloride, then a methylene chloride solution containing 5.4 g of 3,4-dimethoxybenzoyl chloride was added dropwise thereto under ice-cooled condition with stirring. The reaction was continued at the same temperature for 1 hour, then the reaction mixture was washed with water, 5%-sodium bicarbonate aqueous solution, next with potassium carbonate aqueous solution, and was dried. Methylene chloride was removed by distillation, the residue obtained was crystallized by adding ethyl acetate, the crystals formed were collected by filtration. Recrystallized from ethanol to obtain 7.5 g of o-methoxycarbonyl-α-[4-(3,4-dimethoxy-benzoyl)-1-piperazinyl]acetanilide in the form of colorless needle-like crystals. Melting point: 167.5°-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585774
Source datasetuspto-grants-1986_04
ORD IDord-7fd697e16f894d51828b886afb75e08b
Source noteuspto-grants-1986_04