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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767970Generated: October 31, 2026

Ethyl 2-chloroacetoacetate → HCID 69280529, compound

https://huagongshe.com/reaction/1767970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloroacetoacetateHCID 11858—
Reactant2,3-Difluoro-4-(trifluoromethyl)benzene-1-carbothioamideHCID 23614485—
SolventEthanolHCID 702—
ProductHCID 69280529HCID 6928052942%

Reaction Steps

A solution of 2,3-difluoro-4-trifluoromethyl-thiobenzamide (1.15 g, 4.8 mmol) and ethyl 2-chloro-acetoacetate (0.67 ml, 4.8 mmol) in ethanol (70 ml) was heated at reflux temperature for 14 hours. The solvent was removed under reduced pressure and the residue partitioned between ice water and ethyl acetate. The layers were separated and the aqueous phase extracted two more times with ethyl acetate. The combined extracts were washed two times with ice water/brine 1/1 and dried over sodium sulfate. The solvent was removed under reduced pressure to give a yellow oil which was purified by column chromatography (silica gel, heptane/AcOEt) to yield 700 mg (2 mmol, 42%) of the title compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235572B2
Source datasetuspto-grants-2007_06
ORD IDord-eee3dc61cd5d4a0997248e0ee4608ce4
Source noteuspto-grants-2007_06