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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237131Generated: October 31, 2026

Dimethylformamide → HCID 13078278, compound

https://huagongshe.com/reaction/237131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21315212HCID 21315212—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
ProductHCID 13078278HCID 130782781,084.6%

Reaction Steps

A mixture of 2',5-dichloro-2-(3-dimethylcarbamoyl-5-carbobenzoxyaminomethyl-1,2,4-triazol- 1-yl)benzophenone (3.6 g) and 30% hydrogen bromide-acetic acid (9 ml) is stirred at room temperature for 2 hours. The reaction mixture is mixed with ether, and the precipitate is isolated by decantation and washed thrice with ether, whereby 2',5-dichloro-2-(3-dimethylcarbamoyl-5-aminomethyl-1,2,4-triazol- 1-yl)-benzophenone hydrobromide is obtained. This hydrobromide (1.2 g) is added to a solution of chloroacetyl chloride (1.2 g) in benzene (40 ml) to give a solution, which is mixed with dimethylformamide (20 ml). The resultant mixture is stirred at room temperature for 3 hours. The reaction mixture is mixed with ethyl acetate and neutralized with aqueous sodium bicarbonate. The organic layer is separated, washed with water, dried, and evaporated under reduced pressure to remove the solvent. The residue is treated with ethanol/n-hexane to give 2',5-dichloro-2-[3-dimethylcarbamoyl-5-(2-chloroacetylamino)methyl-1,2,4-triazol- 1-yl]-benzophenone (12.9 g), which is recrystallized from ethyl acetate to give colorless needles melting at 80°-82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04159374
Source datasetuspto-grants-1979_06
ORD IDord-ff7876eb624d43b0a45c5b60ce971c9b
Source noteuspto-grants-1979_06