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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47897Generated: October 29, 2026

Acetic Anhydride → HCID 178471883, compound

https://huagongshe.com/reaction/47897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl orthoformateHCID 31214—
ReactantCyclopropylamineHCID 69828—
ReactantEthyl 2,4,6-trichloro-3,5-difluorobenzoylacetateHCID 86589177—
ProductHCID 178471883HCID 17847188374.8%

Reaction Steps

82.9 g of ethyl 2,4,6-trichloro-3,5-difluorobenzoylacetate (0.25 mol), 66.6 g of triethyl orthoformate (0.45 mol) and 77.4 g of diacetyl oxide (0.72 mol) were stirred at 150° C. for 2.5 hours. Fractions having a lower boiling point were evaporated under reduced pressure. To the residue was added 250 ml of anhydrous ethanol. 14.5 g of cyclopropylamine (0.25 mol) was added to the solution under cooling of ice water and the reaction was then carried at room temperature for 2 hours. The resultant mixture was filtered under suction. The residue was re-crystallized from a mixture of petroleum ether and cyclohexane to yield 74.5 g (0.187 mol) of ethyl 2-(2,4,6-trichloro-3,5-difluorobenzoyl)-3-cyclopropylaminoacrylate in 74.6% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699992B2
Source datasetuspto-grants-2004_03
ORD IDord-b89926daf4454c288be859258652d887
Source noteuspto-grants-2004_03