Benzoyl chloride → 5-Benzamido-3-mercapto-1,2,4-triazole
Reaktionsgleichung
[NH2:1][C:2]1[NH:6][N:5]=[C:4]([SH:7])[N:3]=1.[C:8](Cl)(=[O:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>N1C=CC=CC=1>[C:8]([NH:1][C:2]1[NH:6][N:5]=[C:4]([SH:7])[N:3]=1)(=[O:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a suitably equipped reaction vessel was charged 116 g (1.0 mole) of 5-amino-3-mercapto-1,2,4-triazole and 500 mL of pyridine. A total of 147.5 g (1.05 mole) of benzoyl chloride was added with vigorous stirring over 25 min, during which time the temperature rose from 24° to 59° C. The mobile, pale yellow slurry obtained was heated at reflux with stirring. The solid material dissolved and then, after about 40 additional min, a white solid began separating. An additional 200 mL of pyridine was added to aid mixing and the reaction was continued at 117°-122° C. for a total of 7 hr. The thick, white slurry obtained was filtered, washed with water and with methylene chloride, and dried to obtain 186 g (84 percent of theory) of the title compound, m.p. 311°-312° C. (dec.).
Aufarbeitung
- customTo a suitably equipped reaction vessel
- customrose from 24° to 59° C
- customThe mobile, pale yellow slurry obtained
- temperaturewas heated
- temperatureat reflux
- stirringwith stirring
- dissolutionThe solid material dissolved
- customafter about 40 additional min, a white solid began separating
- additionAn additional 200 mL of pyridine was added to aid
- additionmixing
- customwas continued at 117°-122° C. for a total of 7 hr
- customThe thick, white slurry obtained
- filtrationwas filtered
- washwashed with water and with methylene chloride
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-19d66b1ff1c3482fabdcdf22496435db
- Quelldatensatz
- uspto-grants-1990_06
- Patentnummer
- US04937350
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