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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082695Generated: October 31, 2026

Chloroacetic Acid → HCID 57038976, compound

https://huagongshe.com/reaction/2082695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
ReactantChloroacetyl chlorideHCID 6577—
ReactantHCID 20360436HCID 20360436—
SolventBenzeneHCID 241—
ProductHCID 57038976HCID 5703897634%

Reaction Steps

2-Amino-5,2'-dichlorobenzophenone is reacted with formic acid, whereby 5, 2'-dichloro-2-formylaminobenzophenone (pale yellow granules melting at 106° to 107° C) is obtained. The product is then reacted with hydrazine hydrate, whereby 3-amino-6-chloro-4-(2-chlorophenyl)-3,4-dihydro-4-hydroxyquinazoline (colorless granules melting at 198° C (effervescence)) is obtained. The product is reacted with chloroacetyl chloride, whereby a bis-(monochloroacetyl) derivative of 3-amino-6-chloro-4-(2-chlorophenyl)-3,4-dihydro-4-hydroxyquinazoline (colorless powdery crystals melting at 157° to 158° C) is obtained. Further, the product is treated with monochloroacetic acid in dry benzene under refluxing, whereby crystals of 2-(3-chloromethyl-s-triazol-4-yl)-5, 2'-dichlorobenzophenone are obtained. Recrystallization from chloroform-n-hexane gives colorless granules melting at 139° to 140° C. Overall yield: 34%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04082764
Source datasetuspto-grants-1978_04
ORD IDord-6d4a068daa8a4a69afcae1d9df55b5cb
Source noteuspto-grants-1978_04