HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanone, 2-chloro-1,2-diphenyl- → 2-(3,4-Methylenedioxyphenyl)-4,5-diphenylthiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanone, 2-chloro-1,2-diphenyl- | HCID 95343 | — |
| Reactant | 2H-1,3-benzodioxole-5-carbothioamide | HCID 2776126 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(3,4-Methylenedioxyphenyl)-4,5-diphenylthiazole | HCID 20344983 | 67.1% |
Reaction Steps
Thiopiperonylamide (18.1g, 0.10 mole) and desyl chloride (23.1g, 0.10 mole) are heated under reflux in 95% ethanol (100 ml) for two hours. An oil precipitates which solidifies when the reaction mixture is cooled. The solid is collected and recrystallized from ethanolethyl acetate to give 24.0g (67% yield) of 2-(3,4-methylenedioxyphenyl)-4,5-diphenylthiazole, m.p. 121°-124° C. Thiopiperonylamide is also prepared from the corresponding nitrile by the method of Fairfull et al., J. Chem. Soc. 1952, 742.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04153703 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-e5b0204e8488451689e553449c72c4ac |
| Source note | uspto-grants-1979_05 |