Methanethiol → 2-Chloro-6-(methylsulfanyl)pyrazine
Reaktionsgleichung
[Na].[H-].[Na+].[CH3:4][SH:5].[Cl:6][C:7]1[CH:12]=[N:11][CH:10]=[C:9](Cl)[N:8]=1>C1C=CC=CC=1>[Cl:6][C:7]1[CH:12]=[N:11][CH:10]=[C:9]([S:5][CH3:4])[N:8]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
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.
Aufarbeitung
- temperatureat reflux for 24 hours
- temperaturecooled
- washwashed twice with 50 ml
- customThe benzene layer is separated
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- distillationDistillation of the residue
Quellen und Nachweise
- ORD-Eintrag
- ord-51ce95e9ccca438d8bee797a9daa1d48
- Quelldatensatz
- uspto-grants-1978_03
- Patentnummer
- US04081542
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