Triethylamine → 1H-Imidazole-2-carbonitrile, 1-(phenylmethyl)-

温度

-20 °C

In a 50 ml 4-neck flask with stirring bar, nitrogen bubbler, gas inlet tube, thermometer, septum and acetonitrile (20 ml) was bubbled cyanogen chloride (3.1 g, 50 mmol) (ice bath was used to avoid mild heat of solution). The reaction was cooled in an ice bath and a solution of 1-benzylimidazole (3.16 g, 20 mmol) in acetonitrile (ca. 5 ml) was added via syringe. The colorless solution turned yellow-orange and within a few minutes a yellow-orange crystalline solid started to form. After 1 hour, the thick slurry was cooled to -20° C. and triethylamine (7 ml, 50 mmol) was added at such a rate to prevent the temperature from rising above 0° C. The mixture was stirred 1 hour while warming to room temperature, poured into saturated aq NaHCO3 (100 ml) and extracted with ether (3×75 ml). The combined organic layers were dried (MgSO4), evaporated and purified by Kugelrohr distillation. After a forerun of diethylcyanamide, the desired product was collected at 130° C. (0.4 mm) (3.05 g, 83%) as a colorless liquid which crystallized on standing, mp 51°-52° C. (cyclohexane).

1. temperatureThe reaction was cooled in an ice bath
2. waitThe colorless solution turned yellow-orange and within a few minutes
3. customto form
4. customfrom rising above 0° C
5. stirringThe mixture was stirred 1 hour
6. temperaturewhile warming to room temperature
7. extractionextracted with ether (3×75 ml)
8. dry with materialThe combined organic layers were dried (MgSO4)
9. customevaporated
10. distillationpurified by Kugelrohr distillation
11. customAfter a forerun of diethylcyanamide, the desired product was collected at 130° C. (0.4 mm) (3.05 g, 83%) as a colorless liquid which
12. customcrystallized

ORDレコード

ord-a919792284284e34a04a2b1e243f4d59

出典データセット

uspto-grants-1992_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05147863