Reaktionsgleichung
[NH2:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[C:11](N1C=CN=C1)(N1C=CN=C1)=[S:12].C(N(CC)CC)C.Cl>CCCCCCC.C(Cl)Cl>[N:1]([C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6])=[C:11]=[S:12]Komponenten
Reaktionsbedingungen
- Temperatur
- -10 °C
Versuchsvorschrift
3-aminobenzoic acid (5.00 g, 36.5 mmol) was added to a methylene chloride solution (51 mL) of thiocarbonyldiimidazole (7.8 g, 43.8 mmol) and triethylamine (5.6 mL, 40.2 mmol) at an internal temperature of at most 5° C., followed by stirring at −10° C. for one hour. The mixture was dropped to a separately prepared mixed solution of concentrated hydrochloric acid (11.6 mL, 133.0 mmol) and n-heptane (51 mL) as that the internal temperature became from 20° C. to 30° C., followed by stirring for one hour as it was. Then, the mixture was stirred under cooling with ice for 2 hours, and the obtained colorless solid was collected by filtration, washed with water (20 mL) four times and dried under reduced pressure to obtain 3-isothiocyanatobenzoic acid as a creamy solid (6.01 g, yield: 93%, HPLC purity: 99.8%).
Aufarbeitung
- additionThe mixture was dropped to
- customa separately prepared
- custombecame from 20° C. to 30° C.
- stirringby stirring for one hour as it
- stirringThen, the mixture was stirred
- temperatureunder cooling with ice for 2 hours
- filtrationthe obtained colorless solid was collected by filtration
- washwashed with water (20 mL) four times
- customdried under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-78236d238c1240e8b43b6e8c64cfb0f8
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09102602B2
Verknüpfte Notizen
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