HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → HCID 22768209, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Chloro-2-nitrobenzotrifluoride | HCID 67052 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22768209 | HCID 22768209 | — |
Reaction Steps
The sodium salt of methanethiol is formed by stirring a solution of methanethiol (100 g, 2.0 mole plus a slight excess), sodium hydroxide (80 g, 2.0 mole) and ethanol (2 l.) under nitrogen at 0°-5° C. for 1 hour. To this solution is rapidly added 5-chloro-2-nitrobenzotrifluoride (451.2 g, 2.0 mole). The solution is allowed to warm to room temperature overnight and then refluxed four hours, cooled, filtered and the solvent evaporated off under reduced pressure. The resulting oil is poured into cold water (1 l.), extracted with methylene chloride, dried over magnesium sulfate and the solvent evaporated under reduced pressure to afford a yellow solid. Recrystallization from hexane affords a product having a melting point of 47°-50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03996277 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-febcfe2a95be420ab76242d297ff30b9 |
| Source note | uspto-grants-1976_12 |