Sodium Chloride → Anthraquinone

반응식

N[C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:17])[C:6]=2[C:5](SC2C=CC(S(O)(=O)=O)=CC=2)=[CH:4][C:3]=1OC1C=CC(S(O)(=O)=O)=C(N)C=1.N1C(Cl)=NC(Cl)=NC=1Cl.NC1C=C(S(O)(=O)=O)C=CC=1.[Cl-].[Na+]>>[CH:9]1[C:8]2[C:7](=[O:17])[C:6]3[C:15](=[CH:2][CH:3]=[CH:4][CH:5]=3)[C:14](=[O:16])[C:13]=2[CH:12]=[CH:11][CH:10]=1

참가 물질

반응물 4

HCID 5234Sodium Chloride

HCID 7954Cyanuric chloride

HCID 84743-Aminobenzenesulfonic acid

HCID 147173781-Amino-2-(3'-amino-4'-sulfophenoxy)-4-(4-sulfophenylthio)anthraquinone

생성물 1

HCID 6780Anthraquinone

실험 절차

1-Amino-2-(3'-amino-4'-sulfophenoxy)-4-(4'-sulfophenylthio)anthraquinone (6 parts) and cyanuric chloride (1.8 parts) were subjected a to condensation reaction in an aqueous medium in a conventional manner, followed by a condensation reaction with 3-aminobenzenesulfonic acid (1.7 parts) at 20° to 40° C. under a weak acid condition. Thereafter, salting out of the reaction mixture with sodium chloride gave an anthraquinone compound of the following formula (free acid form). ##STR215##