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

HRID 1681532

반응식

HRID 1681532 반응식
[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]

참가 물질

5

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-c6e642d6473f49f289fd4c4ab8dc3d5e
출처 데이터셋
uspto-grants-1992_12
특허 번호
US05171863

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