HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → 1-[5-(Methylsulfanyl)-4-nitrothiophen-2-yl]ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-(5-Chloro-4-nitrothiophen-2-yl)ethan-1-one | HCID 521105 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[5-(Methylsulfanyl)-4-nitrothiophen-2-yl]ethan-1-one | HCID 20213684 | — |
Reaction Steps
Liquid methylmercaptan (4 ml) was added to a solution of 0.82 g of Na in 50 ml of absolute ethanol. The resulting solution was added to a solution of 7.2 g of 2-chloro-3-nitro-5-acetylthiophene in 200 ml of absolute ethanol in 15 minutes at 5° C. After stirring at room temperature for 30 minutes, 100 ml of water was added, after which the precipitate was sucked off and washed successively with water and isopropanol. The precipitate was boiled a moment with 300 ml of carbontetrachloride, cooled down, and sucked off. After drying the title compound was obtained in a yield of 6.4 g; m.p. 191°-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04649154 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-f2f88eeedaa947b58ba2cca4da57948f |
| Source note | uspto-grants-1987_03 |