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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954773Generated: November 1, 2026

Acetic Anhydride → HCID 2823103, compound

https://huagongshe.com/reaction/1954773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantCyanoacetic acidHCID 9740—
ReactantHCID 23293707HCID 23293707—
SolventTolueneHCID 1140—
ProductHCID 2823103HCID 2823103—

Reaction Conditions

Temperature77.5 °C

Reaction Steps

1-(2-Methylphenyl)-3-[2-(methylthio)benzyl]urea(23.47 g) and cyanoacetic acid (7.66 g) were ground together and acetic anhydride (23 ml) was added. The mixture was stirred and heated at 75-80° C. for 30 h. Toluene (20 ml) was then added and heating continued for a further 16 hours. The reaction was cooled and filtered. The filtrate was heated to boiling and treated with charcoal. The solid was removed by filtration and the filtrate evaporated in vacuo. The resulting oil was dissolved in dichloromethane (300 ml) and triethylamine (8.15 g) added. The mixture was stirred for 5 hours at room temperature and the solvent removed in vacuo. The residue was purified by column chromatography on silica gel eluting with ethyl acetate and the product was recrystallised from ethyl acetate. Yield=2.60 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124288
Source datasetuspto-grants-2000_09
ORD IDord-5e8d11b735824f79898186ddd7e60fd7
Source noteuspto-grants-2000_09