HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Nitro-1-phenylethanone → 2-nitro-1-phenyl-2-(tetrahydro-2H-1,3-thiazin-2-ylidene)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Nitro-1-phenylethanone | HCID 94833 | — |
| Reactant | 2-(methylsulfanyl)-5,6-dihydro-4H-1,3-thiazine | HCID 2782081 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | 2-nitro-1-phenyl-2-(tetrahydro-2H-1,3-thiazin-2-ylidene)ethanone | HCID 73179523 | — |
Reaction Steps
A mixture of 3.3 g of 2-nitroacetophenone and 2.94 g of 2-(methylthio)-5,6-dihydro-4H-1,3-thiazine was heated to 115° and 100 milligrams of zinc chloride was added. Heating and stirring was continued at 115°-120° for 2.5 hours. After cooling, the mixture was filtered (with the aid of ethyl acetate) through a short column of florosil to give an amber oil. The oil was chromatographed on silica gel using dry-column technique and a 1:1:2 mixture of tetrahydrofuran/ethyl acetate/hexane for development to give 1 as a salmon-colored solid, m.p.: 137°-140°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03962225 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-c121f869ad254e72aa5ed30b52d0f3d5 |
| Source note | uspto-grants-1976_06 |