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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 358779Erstellt: 25. Oktober 2026

Water → Methyl 4-(4-methoxycinnamoyl)-1(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate

https://huagongshe.com/reaction/358779

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
EduktMethyl 1-(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylateHCID 20066654—
Edukt4-Methoxycinnamic acid chlorideHCID 53401772—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 4-(4-methoxycinnamoyl)-1(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylateHCID 5387843778,9%

Reaktionsschritte

A solution of 4-methoxy cinnamoyl chloride (0.3 g) in dichloromethane (4 ml) is added dropwise, taking 3 minutes at 0 ° C while stirring, to a mixture of methyl 1-(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate (0.57 g), triethylamine (0.4 g) and dichloromethane (12 ml). The reaction mixture is stirred for 30 minutes at room temperature, and then poured into water, followed by extraction with dichloromethane. The organic layer is washed with dilute hydrochloric acid, an aqueous solution of sodium hydrogencarbonate and water, successively, then the solvent is distilled off. The residue is purified by means of a silica gel column chromatography to give methyl 4-(4-methoxycinnamoyl)-1(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate (0.6 g) as a colorless oily product. This product is processed with ethyl ether to give colorless powder

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04997836
Quelldatensatzuspto-grants-1991_03
ORD IDord-c6b2a9131e5340c2968dee10804eb67d
Quellennotizuspto-grants-1991_03