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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Veratroyl chloride | HCID 77070 | — |
| Reactant | o-Methoxycarbonyl-alpha-(1-piperazinyl)acetanilide | HCID 13117362 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | o-Methoxycarbonyl--[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]acetanilide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04585774 |
|---|
| Source dataset | uspto-grants-1986_04 |
|---|
| ORD ID | ord-7fd697e16f894d51828b886afb75e08b |
|---|
| Source note | uspto-grants-1986_04 |
|---|