HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 18427783, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | [2,6-Dichloro-4-(trifluoromethyl)phenyl]hydrazine | HCID 688223 | — |
| Reactant | HCID 18427784 | HCID 18427784 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18427783 | HCID 18427783 | 40.2% |
Reaction Steps
A suspension of 0.50 g (1.42 mmol) of 3,3-bis-methylthio-2-(3-trifluoromethylphenylsulfonyl)acrylonitrile and 0.35 g (1.42 mmol) of 2,6-dichloro-4-trifluoromethylphenylhydrazine in 10 mL of ethanol was heated at reflux for 2.5 hours, solution occurring as the reaction mixture was warmed. The mixture was stirred overnight at room temperature and was then poured into cold water. The product was extracted into ethyl acetate and the extracts were dried with magnesium sulfate and evaporated. The residues were crystallized from ether, and the product was filtered off and air dried to give 314 mg (40%) of the desired product, m.p. 201°-203° C. Anal. Calcd. for C18H11O2N3S2Cl2F6 : C, 39.28; H, 2.02; N, 7.64. Found: C, 39.35; H, 2.19; N, 7.48.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05712303 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-104d1e8f63514cb5820a7e0e79b1e77c |
| Source note | uspto-grants-1998_01 |