Acetic Anhydride → 3(-1-Acetoxytridecyl)-4-phenylfuran

HRID 273957

反応式

HRID 273957 の反応式
[CH2:1]([Mg]Br)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[C:15]1([C:21]2[C:22]([CH:26]=[O:27])=[CH:23][O:24][CH:25]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[C:28](OC(=O)C)(=[O:30])[CH3:29]>C1COCC1>[C:28]([O:27][CH:26]([C:22]1[C:21]([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)=[CH:25][O:24][CH:23]=1)[CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])(=[O:30])[CH3:29]

参加物

5

実験手順

Dodecylmagnesium bromide (a 1.0M solution in THF; 2.11 ml, 2.11 mmol) was added to a solution of 4-phenyl-3-furaldehyde (303 mg, 1.76 mmol) in THF at 0 degrees under argon and gradually allowed to warm to room temperature with stirring. When all of the aldehyde was consumed acetic anhydride (719 mg, 7.04 mmol) was added and stirring was continued for 2 hours more. The reaction was quenched with saturated ammonium chloride and the organics were extracted into ethyl ether. The combined fractions were washed with saturated sodium bicarbonate, water and brine, dried over magnesium sulfate and concentrated to a yellow oil which was purified by flash chromatography on silica using 3% ethyl ether hexanes to give the title compound.

後処理

  1. additionwas added
  2. stirringstirring
  3. customThe reaction was quenched with saturated ammonium chloride
  4. extractionthe organics were extracted into ethyl ether
  5. washThe combined fractions were washed with saturated sodium bicarbonate, water and brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated to a yellow oil which
  8. customwas purified by flash chromatography on silica using 3% ethyl ether hexanes

出典と根拠

ORDレコード
ord-b1812e3a919a44a88201410d57a6b28c
出典データセット
uspto-grants-1995_02
特許番号
US05387606

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