Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531401Generated: October 26, 2026

Dimethylformamide → 2,4,5-Trimethoxybenzoyl chloride

https://huagongshe.com/reaction/1531401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2,4,5-Trimethoxybenzoic acidHCID 10276—
ReactantThionyl ChlorideHCID 24386—
SolventTolueneHCID 1140—
Product2,4,5-Trimethoxybenzoyl chlorideHCID 2760809—

Reaction Conditions

Temperature80 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197970B1
Source datasetuspto-grants-2001_03
ORD IDord-2f6b994fe6884d4b857c2644854f0d2c
Source noteuspto-grants-2001_03