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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5357Generated: October 27, 2026

Methyl iodide → 3-Ethoxycarbonyl-2-methylthio-4-oxo-6,7,8-trifluoro-4H-1-benzothiopyran

https://huagongshe.com/reaction/5357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
ReactantEthyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 600916—
SolventDimethyl SulfoxideHCID 679—
Product3-Ethoxycarbonyl-2-methylthio-4-oxo-6,7,8-trifluoro-4H-1-benzothiopyranHCID 2177022274%

Reaction Steps

To a solution of 3.00 g (11.4 mmol) of ethyl 2,3,4,5-tetrafluorobenzoylacetate, 870 mg (11.4 mmol) of carbon disulfide and 9 ml of dried dimethyl sulfoxide were added 2.31 g (22.8 mmol) of triethylamine at room temperature, and the mixture was stirred for 1 hour at room temperature. Then, at room temperature, 3.24 g (22.8 mmol) of methyl iodide were added and the mixture was stirred for 2 hours, which was poured into ice-water. The crystals deposited were collected by filtration and dried to obtain 2.81 g (8.41 mmol) of title compound (yield 74%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244892
Source datasetuspto-grants-1993_09
ORD IDord-93c2e2181a674049914d3893aea5bed6
Source noteuspto-grants-1993_09