HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → HCID 10156540, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(2-Isopropylphenyl)imino-5,5-dimethyl-1,3-thiazine | HCID 22379500 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10156540 | HCID 10156540 | 69% |
Reaction Steps
To a solution of 2-(2-isopropylphenyl)imino-5,5-dimethyl-1,3-thiazine (0.26 g), carbondisulfide (0.10 g) in N,N-dimethylformamide (3 ml) was added 60% sodium hydride (0.05 g) under ice-cooling. The reaction mixture was stirred for 30 minutes. Allylchloride (0.10 g) was added thereto. The reaction mixture was stirred at 0° C. for 1 h. To a reaction mixture was added water (80 ml), extracted with diethylether (100 ml), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to give 2-(2-isopropylphenyl)imino-3-(allylthio)thiocarbonyl-5,5-dimethyl-1,3-thiazine (0.26 g, yield: 69%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06916806B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-0e7b6afbbaf947f5815899b202fc17b4 |
| Source note | uspto-grants-2005_07 |