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2,3-Dichloroaniline → 2-amino-4,5-dichlorobenzothiazole

HRID 1882881
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1882881
[Cl:1][C:2]1[C:8]([Cl:9])=[CH:7][CH:6]=[CH:5][C:3]=1[NH2:4].[S-:10][C:11]#[N:12].[K+].BrBr>C(O)(=O)C>[NH2:12][C:11]1[S:10][C:5]2[CH:6]=[CH:7][C:8]([Cl:9])=[C:2]([Cl:1])[C:3]=2[N:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 118442,3-DichloroanilineHCID 24408BromineHCID 516872Potassium thiocyanate

Produkt 1

HCID 6677392-amino-4,5-dichlorobenzothiazole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

To a solution of 2,3-dichloroaniline (1.0 g; 6.17 mmol) in glacial acetic acid (30 ml) was added potassium thiocyanate (3.6 g; 37 mmol) and the mixture was stirred at ambient temperature until a clear solution had formed. Bromine (0.48 ml; 9.26 mmol) was added dropwise and the reaction mixture was stirred at ambient temperature for five hours. The solvent was removed under reduced pressure and the residue was diluted with water and rendered alkaline by addition of aqueous sodium hydroxide (6M). The product was filtered off, washed with water and dried to yield the desired product quantitatively.

Aufarbeitung

  1. customhad formed
  2. stirringthe reaction mixture was stirred at ambient temperature for five hours
  3. customThe solvent was removed under reduced pressure
  4. additionthe residue was diluted with water
  5. additionby addition of aqueous sodium hydroxide (6M)
  6. filtrationThe product was filtered off
  7. washwashed with water
  8. customdried

Quellen und Nachweise

ORD-Eintrag
ord-9760a974e5f24c6b88d727b803e4bba9
Quelldatensatz
uspto-grants-2004_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06759422B2

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