Dimethylformamide → HCID 86622730、化合物

HRID 2410343ノート

反応式

HRID 2410343 の反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH2:9][CH:10]([CH3:12])[CH3:11])[CH:3]=1.[Li]C(CC)C.CN(C)[CH:20]=[O:21]>O1CCCC1>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH2:9][CH:10]([CH3:12])[CH3:11])[C:3]=1[CH:20]=[O:21]

参加物

5

反応条件

温度
-20 °C

実験手順

To a solution of 1-fluoro-3-isobutoxybenzene (1.7 g, 10 mmol, EXAMPLE 16, Step 1) in tetrahydrofuran (15 mL) was added dropwise s-BuLi (0.99 M in cyclohexane, 12 mL, 12 mmol) at −78° C. under nitrogen atmosphere, and the mixture was stirred for 1 h. N,N-dimethylformamide (1.2 mL, 15 mmol) was added to the mixture, and the mixture was warm to −20° C. After being stirred at −20° C. for 1 h, the mixture was quenched with aq. sodium hydrogencarbonate (30 mL). The mixture was extracted with ethyl acetate (60 mL) and washed with water (30 mL). The extract was dried over magnesium sulfate and concentrated in vacuo to give an oil. The residual oil was purified by silica gel column chromatography (hexane/ethyl acetate 30:1) to give 1.2 g (61%) of the title compound as a colorless oil.

後処理

  1. stirringAfter being stirred at −20° C. for 1 h
  2. customthe mixture was quenched with aq. sodium hydrogencarbonate (30 mL)
  3. extractionThe mixture was extracted with ethyl acetate (60 mL)
  4. washwashed with water (30 mL)
  5. dry with materialThe extract was dried over magnesium sulfate
  6. concentrationconcentrated in vacuo
  7. customto give an oil
  8. customThe residual oil was purified by silica gel column chromatography (hexane/ethyl acetate 30:1)

出典と根拠

ORDレコード
ord-40083fa9a0b94013830e6af23c0a971b
出典データセット
uspto-grants-2014_08
特許番号
US08816090B2

反応ノート

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