HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → 2-Chloro-6-(methylsulfanyl)pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,6-Dichloropyrazine | HCID 78504 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Chloro-6-(methylsulfanyl)pyrazine | HCID 20361685 | — |
Reaction Steps
A mixture of 0.13 mole of sodium methylmercaptide (prepared from 3.12 g. sodium hydride and excess methyl mercaptan), 20 g. (0.13 mole) of 2,6-dichloropyrazine and 200 ml. benzene is heated at reflux for 24 hours, cooled and washed twice with 50 ml. water. The benzene layer is separated, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Distillation of the residue gives 2-chloro-6-methylthiopyrazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04081542 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-51ce95e9ccca438d8bee797a9daa1d48 |
| Source note | uspto-grants-1978_03 |