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Hydrochloric Acid → 2-(4-(Difluoromethoxy)phenyl)acetaldehyde

HRID 1992386
ノート
印刷プレビュー

反応式

HRID 1992386 の反応式
[F:1][CH:2]([F:14])[O:3][C:4]1[CH:9]=[CH:8][C:7]([CH:10]=[CH:11][O:12]C)=[CH:6][CH:5]=1.Cl>CC(C)=O>[F:1][CH:2]([F:14])[O:3][C:4]1[CH:5]=[CH:6][C:7]([CH2:10][CH:11]=[O:12])=[CH:8][CH:9]=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

4

反応物 2

HCID 313Hydrochloric AcidHCID 685206391-Difluoromethoxy-4-((EZ)-2-methoxy-vinyl)-benzene

生成物 1

HCID 592595402-(4-(Difluoromethoxy)phenyl)acetaldehyde収率 89.8%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

反応条件

温度
45 °C

実験手順

To a solution of 1-difluoromethoxy-4-((E,Z)-2-methoxyvinyl)-benzene (E/Z ratio ˜3:2,) (1.58 g, 7.9 mmol, from step (i) above ) in acetone (20 mL) was added 3 M HCl (3.7 mL, 11.1 mmol) and the solution was stirred at 45° C. for 4 h. After concentration under reduced pressure, water (25 mL) was added to the residue and the aqueous phase was extracted with diethylether (2×50 mL). The combined organic phase was washed with saturated aqueous NaHCO3 (50 mL) and brine (50 mL), dried over Na2SO4, and concentrated in vacuo to give 1.32 g of crude product as a yellow oil with a purity of ca. 80%. The crude product was used directly in the subsequent reduction step without further purification.

後処理

  1. concentrationAfter concentration under reduced pressure, water (25 mL)
  2. additionwas added to the residue
  3. extractionthe aqueous phase was extracted with diethylether (2×50 mL)
  4. washThe combined organic phase was washed with saturated aqueous NaHCO3 (50 mL) and brine (50 mL)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-2f6afdf111704678b54a5fd4d4576e9a
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07648985B2

反応ノート

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