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Phosphorus pentachloride → alpha-chloro-2-(2,4-dichlorobenzyloxy)benzaldehyde O-methyloxime

HRID 128903
ノート
印刷プレビュー

反応式

HRID 128903 の反応式
[Cl:1][C:2]1[CH:20]=[C:19]([Cl:21])[CH:18]=[CH:17][C:3]=1[CH2:4][O:5][C:6]1[CH:16]=[CH:15][CH:14]=[CH:13][C:7]=1[C:8]([NH:10][O:11][CH3:12])=O.P(Cl)(Cl)(Cl)(Cl)[Cl:23].C(=O)(O)[O-].[Na+]>C(Cl)Cl>[CH3:12][O:11][N:10]=[C:8]([Cl:23])[C:7]1[CH:13]=[CH:14][CH:15]=[CH:16][C:6]=1[O:5][CH2:4][C:3]1[CH:17]=[CH:18][C:19]([Cl:21])=[CH:20][C:2]=1[Cl:1]
参加物反応条件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 24819Phosphorus pentachlorideHCID 516892Sodium BicarbonateHCID 229044802-(2,4-Dichlorobenzyloxy)-N-methoxybenzamide

生成物 1

HCID 53754588alpha-chloro-2-(2,4-dichlorobenzyloxy)benzaldehyde O-methyloxime収率 86.4%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

2-(2,4-Dichlorobenzyloxy)-N-methoxybenzamide (10.44 g) was dissolved in dry methylene chloride (100 ml), phosphorus pentachloride (6.66 g) was added under ice-cooling over about 3 minutes to the solution, and the mixture was stirred at 0° C. for 1 hour. After completion of the reaction, a saturated aqueous solution of sodium bicarbonate (150 ml) was added slowly, and the mixture was extracted with methylene chloride (150 ml) twice, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting crude product was purified by silica gel chromatography to give α-chloro-2-(2,4-dichlorobenzyloxy)benzaldehyde O-methyloxime (9.52 g) as crystals. A part of the crystals was recrystallized from ethyl acetate/n-hexane to give colorless crystals. mp 91°-92° C.

後処理

  1. temperaturecooling over about 3 minutes to the solution
  2. customAfter completion of the reaction
  3. extractionthe mixture was extracted with methylene chloride (150 ml) twice
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe resulting crude product was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-86d81d53fe034b8f985070df8221e077
出典データセット
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05466661

反応ノート

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