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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1531401Erstellt: 25. Oktober 2026

Dimethylformamide → 2,4,5-Trimethoxybenzoyl chloride

https://huagongshe.com/reaction/1531401

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt2,4,5-Trimethoxybenzoic acidHCID 10276—
EduktThionyl ChlorideHCID 24386—
LösungsmittelTolueneHCID 1140—
Produkt2,4,5-Trimethoxybenzoyl chlorideHCID 2760809—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

2,4,5-Trimethoxybenzoic acid (500 g) was suspended in dried toluene (2 l) and to the suspension, thionyl chloride (206 ml) and N,N-dimethylformamide (1.0 ml) were added at room temperature, and the mixture was stirred at 80° C. for 1 hour. The reaction mixture was concentrated under reduced pressure. To the resultant residue, n-hexane was added and through co-boiling the mixture, 2,4,5-trimethoxybenzoyl chloride was obtained. To the resultant compound, 2-amino-4-methoxycarbonyl-1,3-thiazole (372.7 g) and 1,2-dichloroethane (4.5 l) were added and the mixture was refluxed for 6 hours. After completion of reaction, the reaction mixture was allowed to cool. Crystals so precipitated were collected by filtration, washed with 1,2-dichloroethane, and air-dried. The crystals were suspended in water (8 l) and to the suspension, ice (2 kg) was added. While cooling, a solution of sodium hydroxide (94 g) in water (850 ml) was added thereto to thereby adjust the pH of the suspension at about 7.5. Subsequently, the mixture was stirred for 3 hours at room temperature. Crystals so precipitated were collected by filtration, washed with water, and air-dried to thereby obtain the title compound (702.7 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06197970B1
Quelldatensatzuspto-grants-2001_03
ORD IDord-2f6b994fe6884d4b857c2644854f0d2c
Quellennotizuspto-grants-2001_03