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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382734Generated: November 2, 2026

Carbon Disulfide → N,N-diethyl-1-ethanaminium N-(2,3,4-trifluorophenyl)carbamodithioate

https://huagongshe.com/reaction/1382734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
Reactant2,3,4-TrifluoroanilineHCID 77468—
ProductN,N-diethyl-1-ethanaminium N-(2,3,4-trifluorophenyl)carbamodithioateHCID 16413959—

Reaction Steps

That is, first 2,3,4-trifluoroaniline (V) is reacted with carbon disulfide in the presence of triethylamine to produce triethylammonium N-(2,3,4-trifluorophenyl)dithiocarbamate (VI). Then the compound (VI) is reacted with ethyl chloroformate in an organic solvent such as chloroform or methylene chloride in the presence of triethylamine to give 2,3,4-trifluorophenylisothiocyanate (VII). The compound (VII) is then reacted with di(lower alkyl) malonate sodium salt, which is prepared from di(lower alkyl) malonate and sodium hydride, in an organic solvent such as tetrahydrofuran or dioxane to give di(lower alkyl) [(2,3,4-trifluoroanilino)(mercapto)methylene]malonate sodium salt (VIII). The compound (VIII) is then reacted with 1-acetoxy-3-halogenoacetone in an organic solvent such as N,N-dimethylformamide, dimethylsulfoxide or acetonitrile to give di(lower alkyl) [(2,3,4-trifluoroanilino)(3-acetoxy-2-oxopropylthio)methylene]malonate (IX). The compound (IX) is then reacted with sulfuric acid to give di(lower alkyl) [3-(2,3,4-trifluorophenyl)-4-hydroxymethyl-2-thiazolidene]malonate (X). The compound (X) is then reacted with sodium hydride in an organic solvent such as dioxane, tetrahydrofuran or N,N-dimethylformamide to give di(lower alkyl) (6,7-difluoro-1H,4H-thiazolo[4,3-c][1,4]benzoxazin-1-ylidene)malonate (XI).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808584
Source datasetuspto-grants-1989_02
ORD IDord-6e4d341b3c7a4ecd91447f57ee4f5e15
Source noteuspto-grants-1989_02