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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357754Generated: October 31, 2026

Triethylamine → HCID 18187088, compound

https://huagongshe.com/reaction/1357754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Aminocyclohex-2-en-1-oneHCID 78892—
Reactantdihydrothiophen-3(2H)-one 1,1-dioxideHCID 5150067—
Reactant3-NITRO-4-(TRIFLUOROMETHYL)BENZALDEHYDE&HCID 11127762—
SolventEthanolHCID 702—
ProductHCID 18187088HCID 1818708849.8%

Reaction Steps

20 3-Nitro-4-trifluoromethylbenzaldehyde (0.33 g, 1.5 mmol) (Clark, J. Fluorine Chem. 1990, 50, 411), tetrahydrothiophene-3-oxo-1,1-dioxide (0.2 g, 1.5 mmol) and 3-amino-2-cyclohexene-1-one(0. 17 g, 1.5 mmol) in ethanol (2 mL) were heated at reflux for 48 hours with triethylamine (0.1 mL). The reaction mixture was evaporated in vacuo and the residue was chromatographed on silica gel, eluting with 10% ethanol/methylene 25 chloride to afford 0.32 g of the intermediate hemiaminal that was suspended in ethanol (10 mL) and heated at reflux for 2 hours with 2 mL of I M HCUether. The reaction mixture was cooled and the precipitate collected to provide 0.24 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593335B1
Source datasetuspto-grants-2003_07
ORD IDord-75d3b8fb9cec4123b79a8cd3217f49e5
Source noteuspto-grants-2003_07