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Acetic Acid → 1-(4-Fluorophenyl)-4-methylpent-1-en-3-one

HRID 704743
노트
인쇄 미리보기

반응식

HRID 704743 반응식
[OH-].[K+].[F:3][C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1.[CH:12]([C:15]([CH3:17])=[O:16])([CH3:14])[CH3:13].C(O)(=O)C>CO.O>[F:3][C:4]1[CH:11]=[CH:10][C:7]([CH:8]=[CH:17][C:15](=[O:16])[CH:12]([CH3:14])[CH3:13])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 112513-Methyl-2-butanoneHCID 14797Potassium HydroxideHCID 680234-Fluorobenzaldehyde

생성물 1

HCID 537214671-(4-Fluorophenyl)-4-methylpent-1-en-3-one

시약·촉매·용매 2

HCID 887Methanol용매
HCID 962
Water
용매

실험 절차

75 ml of 15% strength potassium hydroxide solution are added dropwise to 198.4 g (1.6 mol) of freshly distilled 4-fluorobenzaldehyde and 137.6 g (1.6 mol) of methyl isopropyl ketone in 300 ml of methanol and the mixture is stirred overnight at room temperature. It is then neutralized using 10 ml of acetic acid, 1 l of water is added and the mixture is extracted using two 500 ml portions of ether. The combined organic phases are washed with 500 ml of saturated sodium chloride solution and dried over sodium sulphate. After stripping off the solvent, the residue is distilled in a high vacuum.

후처리

  1. additionis added
  2. extractionthe mixture is extracted
  3. washThe combined organic phases are washed with 500 ml of saturated sodium chloride solution
  4. dry with materialdried over sodium sulphate
  5. distillationthe residue is distilled in a high vacuum

출처 및 근거

ORD 기록
ord-9773d333a19e499ca576a1866e57fa31
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04988711

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