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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579729Generated: November 2, 2026

Chloroacetic Acid → HCID 68144690, compound

https://huagongshe.com/reaction/1579729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
ReactantO-XyleneHCID 7237—
ReactantHCID 68141832HCID 68141832—
SolventTriethylamineHCID 8471—
ProductHCID 68144690HCID 68144690104%

Reaction Steps

4.6 g of 2-(methylamino-acetamido)-5-chlorobenzophenone hydrochloride were heated in 100 mls. of dry xylene with 3 g of triethylamine and 1.9 g of chloracetic acid for 8 hours under reflux whilst stirring. After cooling, the precipitated triethylamine hydrochloride was filtered off and the filtrate was shaken 3 times with 100 mls. of water each time. After drying over potassium carbonate and filtering, it was concentrated in vacuo, the oily crude base obtained being dissolved in 100 mls. of dry ether and filtered again. By passing in dry hydrogen chloride gas, filtering under suction and drying in a vacuum desiccator, 2.8 g (71% of theory) of 2-(4-carboxy-3-methyl-3-aza-butyramido)-5-chlorobenzophenone hydrochloride were obtained with a melting point of 162°-164°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931301
Source datasetuspto-grants-1976_01
ORD IDord-f3bc41f059af45d9b5404c1889f4b7bb
Source noteuspto-grants-1976_01