HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Ethylthio-5-methyl-6-ethoxycarbonyl-8-chlorothiochroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,8-Dichloro-5-methyl-6-ethoxycarbonylthiochroman | HCID 22118389 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Ethylthio-5-methyl-6-ethoxycarbonyl-8-chlorothiochroman | HCID 22118460 | 139.5% |
Reaction Steps
0.8 Gram (2.6 mmol) of 4,8-dichloro-5-methyl-6-ethoxycarbonylthiochroman was dissolved in 5 ml of N,N-dimethylformamide, and 0.15 ml (3.1 mmol) of ethanethiol and 0.43 g (3.1 mmol) of potassium carbonate were added. The mixture was stirred at room temperature for 2 days. After the completion of the reaction, 20 ml of water was added, and the reaction mixture was extracted with ethyl acetate twice. An organic layer was washed with water and with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate, and the solvent was distilled off to give 1.2 g (yield 100%) of 4-ethylthio-5-methyl-6-ethoxycarbonyl-8-chlorothiochroman.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06159904 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-45552dfeec094c4b80d0b9b39424fe67 |
| Source note | uspto-grants-2000_12 |