Tetrahydrofuran → 1-Chloro-2-fluoro-4-vinylbenzene

HRID 2365788ノート

反応式

HRID 2365788 の反応式
[H-].[Na+].[Cl:3][C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][C:5]=1[F:12].[CH2:13]1COCC1>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[Cl:3][C:4]1[CH:11]=[CH:10][C:7]([CH:8]=[CH2:13])=[CH:6][C:5]=1[F:12]

参加物

5

実験手順

Sodium hydride (8.549 g, 213.7 mmol, 60% suspension in mineral oil) was added portionwise to a cold (0° C.) solution of 4-chloro-3-fluorobenzaldehyde (26.07 g, 164.4 mmol) and methyltriphenylphosphonium bromide (70.48 g, 197.3 mmol) in THF (400 mL). The reaction mixture was allowed to warm up to room temperature overnight. The solids were removed by filtration, and the filter cake was washed with ether. The filtrate was concentrated (water bath about 20° C.), and the residue was suspended in hexanes and stirred for 30 minutes. The solids (mostly PPh3O) were removed by filtration, and the filter cake was washed with hexanes. The filtrate was concentrated, and the crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (25:1) to give 1-chloro-2-fluoro-4-vinylbenzene (12.1 g, 47%) as an oil. 1H NMR (400 MHz, CDCl3) δ 7.33 (m, 1H), 7.18 (m, 1H), 7.10 (m, 1H), 6.63 (m, 1H), 5.74 (d, J=17.4 Hz, 1H), 5.32 (d, J=10.8 Hz, 1H).

後処理

  1. customThe solids were removed by filtration
  2. washthe filter cake was washed with ether
  3. concentrationThe filtrate was concentrated (water bath about 20° C.)
  4. customThe solids (mostly PPh3O) were removed by filtration
  5. washthe filter cake was washed with hexanes
  6. concentrationThe filtrate was concentrated
  7. customthe crude product was purified by column chromatography
  8. washeluting with hexanes/ethyl acetate (25:1)

出典と根拠

ORDレコード
ord-c1482022cc9745cc9044a51fda48e707
出典データセット
uspto-grants-2014_04
特許番号
US08697715B2

反応ノート

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