2-Methylbenzothiazole → 2-(2'-Chloro-5'-nitrostyryl)benzothiazole

HRID 280684

Reaktionsgleichung

Reaktionsgleichung von HRID 280684
[Cl:1][C:2]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][C:3]=1[CH:4]=O.[CH3:13][C:14]1[S:15][C:16]2[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=2[N:18]=1>C(OC(=O)C)(=O)C>[Cl:1][C:2]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][C:3]=1[CH:4]=[CH:13][C:14]1[S:15][C:16]2[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=2[N:18]=1

Komponenten

4

Edukt 2

HCID 84462-MethylbenzothiazoleHCID 729332-Chloro-5-nitrobenzaldehyde

Produkt 1

HCID 541134682-(2'-Chloro-5'-nitrostyryl)benzothiazoleAusbeute 70 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 7918Acetic AnhydrideLösungsmittel

Versuchsvorschrift

A solution of 12.4 g (67 mmol) of 2-chloro-5-nitrobenzaldehyde and 10.0 g (67 mmol) of freshly distilled 2-methylbenzothiazole in 60 ml of acetic anhydride was refluxed for 5 h. The precipitated yellow solid was collected by filtration and recrystallized from toluene to afford 14.9 g (70%) of 2-(2'-chloro-5'-nitrostyryl)benzothiazole (IIIa); mp 188°-189° C., UV λmaxEtOH nm (ε) 214(16808), 332.5(28445); 1H-NMR δTMSCDCl3 (ppm) 8.58 (d, J=2.7 Hz, 1H), 8.16-7.26 (complex pattern, 8H); 13C--NMRTMS δTMSDMSO-d6 (ppm) 165.0, 154.0, 147.1, 140.2, 135.3, 134.9, 131.1, 130.7, 127.3, 126.7, 126.0, 124.0, 123.6, 121.6, 121.0; IR νmaxKbr (cm-1) 1521.8, 1455.4, 1342.4, 1116.3, 1046.3, 951.3, 873.34, 826.1, 724.1, 737.4, 728.3. Anal. Calcd. for C15H9CiN2O2 : C, 56.87, H, 2.86, N, 8.84; Found: C, 56.84; H, 2.86, N, 8.73.

Aufarbeitung

  1. filtrationThe precipitated yellow solid was collected by filtration
  2. customrecrystallized from toluene

Quellen und Nachweise

ORD-Eintrag
ord-48666d7fe91f489e9019e3ed039ed2fc
Quelldatensatz
uspto-grants-1986_05
Patentnummer
US04590275

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