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Phthalic Anhydride → 2-(2,4-Dichlorobenzoyl)benzoic acid

HRID 615663
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 615663
[C:1]1(=[O:11])[O:6][C:4](=[O:5])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[Cl:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[CH:14]=1.[Cl-].[Al+3].[Cl-].[Cl-]>O>[Cl:12][C:13]1[CH:14]=[C:15]([Cl:19])[CH:16]=[CH:17][C:18]=1[C:4]([C:3]1[CH:7]=[CH:8][CH:9]=[CH:10][C:2]=1[C:1]([OH:6])=[O:11])=[O:5]
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Komponenten

5

Edukt 3

HCID 6811Phthalic AnhydrideHCID 109431,3-DichlorobenzeneHCID 6451240Aluminum(III) Chloride

Produkt 1

HCID 3504822-(2,4-Dichlorobenzoyl)benzoic acidAusbeute 54,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To a solution prepared by adding 30 g (0.2 mol.) of phthalic anhydride to 146 g (1.0 mol.) of dried 1,3-dichlorobenzene, was added 64 g (0.48 mol.) of well-ground anhydrous aluminium chloride with stirring. The mixture was heated and stirred for 3 hours on the oil bath kept at 120° C. Thereafter, the reaction mixture was sufficiently cooled on an ice bath and thereto, 100 ml of water was added dropwise. The thus produced white precipitate was thoroughly washed with successive, water and cooled ethanol to obtain 32 g of crude crystals. These crude crystals were recrystallized from benzene to obtain the marked compound. Yield 24 g, Melting Point 178° to 181° C.

Aufarbeitung

  1. customTo a solution prepared
  2. temperatureThe mixture was heated
  3. stirringstirred for 3 hours on the oil bath
  4. customkept at 120° C
  5. temperatureThereafter, the reaction mixture was sufficiently cooled on an ice bath
  6. washThe thus produced white precipitate was thoroughly washed with successive, water
  7. temperaturecooled ethanol

Quellen und Nachweise

ORD-Eintrag
ord-b3e2bbf23be64323b70ccb89148efd25
Quelldatensatz
uspto-grants-1985_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04500636

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