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

HRID 615663
ノート
印刷プレビュー

反応式

HRID 615663 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 3504822-(2,4-Dichlorobenzoyl)benzoic acid収率 54.2%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-b3e2bbf23be64323b70ccb89148efd25
出典データセット
uspto-grants-1985_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04500636

反応ノート

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