4-Bromobenzoic acid → 5-Bromo-2-(4-bromophenyl)-1,3-benzothiazole

HRID 1903555Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1903555
Cl.[Br:2][C:3]1[CH:8]=[CH:7][C:6]([SH:9])=[C:5]([NH2:10])[CH:4]=1.[Br:11][C:12]1[CH:20]=[CH:19][C:15]([C:16](O)=O)=[CH:14][CH:13]=1.O.CO>S1(CCCC1)(=O)=O>[Br:11][C:12]1[CH:20]=[CH:19][C:15]([C:16]2[S:9][C:6]3[CH:7]=[CH:8][C:3]([Br:2])=[CH:4][C:5]=3[N:10]=2)=[CH:14][CH:13]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

A mixture of 20 g (0.083 mole) of 4-bromo-2-aminothiophenol hydrochloride and 270 g of deoxygenated polyphosphoric acid was heated at 70° C. for 4 hours. To this mixture was added a solution containing 22 g (0.11 mole) of p-bromobenzoic acid dissolved in 109 g of sulfolane. The reaction mixture was slowly heated to 200° C. and maintained at that temperature for 1 hour. After cooling, the reaction mixture was poured into a 1:1 water-methanol solution to precipitate the product. The light tan precipitate was filtered, washed with dilute ammonium hydroxide, washed with water, and then air dried. The 2-(4-bromophenyl)-5-bromobenzothiazole was recrystallized from toluene to give 24.5 g (80% of theoretical), m.p. 162°-163° C.

Aufarbeitung

  1. additionTo this mixture was added a solution
  2. temperatureThe reaction mixture was slowly heated to 200° C.
  3. temperaturemaintained at that temperature for 1 hour
  4. temperatureAfter cooling
  5. customto precipitate the product
  6. filtrationThe light tan precipitate was filtered
  7. washwashed with dilute ammonium hydroxide
  8. washwashed with water
  9. customair dried
  10. customThe 2-(4-bromophenyl)-5-bromobenzothiazole was recrystallized from toluene
  11. customto give 24.5 g (80% of theoretical), m.p. 162°-163° C.

Quellen und Nachweise

ORD-Eintrag
ord-107440b7545845ca9d5a7430b8a8b596
Quelldatensatz
uspto-grants-1984_03
Patentnummer
US04436886

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