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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452806Generated: October 26, 2026

Carbon Disulfide → HCID 178506378, compound

https://huagongshe.com/reaction/452806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-[3-(Trifluoromethoxy)phenyl]-1-benzofuran-5-carbohydrazideHCID 68664388—
SolventEthanolHCID 702—
ProductHCID 178506378HCID 178506378—

Reaction Steps

A mixture of the obtained 3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-carbohydrazide, triethylamine (5.6 mL, 40.4 mmol), carbon disulfide (18.2 mL, 303 mmol) and ethanol (70 mL) was heated under reflux for 5 hr. After cooling, saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1-1/2) and recrystallized from hexane/ethyl acetate to give 5-[3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole-2-thiol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-fba1d2cc8d5d4287b2273c83ed9c279d
Source noteuspto-grants-2013_07