Potassium Carbonate → Ethyl 4,5-dichloro-1,3-benzodioxole-2-carboxylate

HRID 1089171Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1089171
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[C:4]([OH:9])[C:3]=1[OH:10].C(=O)([O-])[O-].[K+].[K+].Br[CH:18](Br)[C:19]([O:21][CH2:22][CH3:23])=[O:20]>CN(C)C=O>[Cl:1][C:2]1[C:3]2[O:10][CH:18]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[O:9][C:4]=2[CH:5]=[CH:6][C:7]=1[Cl:8]

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 198773,4-DichlorocatecholHCID 69237Ethyl dibromoacetate

Produkt 1

HCID 14748637Ethyl 4,5-dichloro-1,3-benzodioxole-2-carboxylateAusbeute 66,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A mixture of 11.0 g of 3,4-dichloro-1,2-benzenediol, 15.38 g of potassium carbonate, 27 g of ethyl dibromoacetate and 100 ml of dimethylformamide is stirred at 100° C. under argon gas atmosphere for 4 hours. The reaction mixture is evaporated to remove solvent and ethyl acetate and water is added to the residue. The organic layer is separated, washed with water, dried and evaporated to remove solvent. The residue is purified by silica gel column chromatography to give 10.75 g of ethyl 4,5-dichloro-1,3-benzodioxole-2carboxylate.

Aufarbeitung

  1. customThe reaction mixture is evaporated
  2. customto remove solvent and ethyl acetate and water
  3. additionis added to the residue
  4. customThe organic layer is separated
  5. washwashed with water
  6. customdried
  7. customevaporated
  8. customto remove solvent
  9. customThe residue is purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-9075ba1993954ec9ab3cfa7defecb40b
Quelldatensatz
uspto-grants-1990_10
Patentnummer
US04965282

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