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

HRID 1073094
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인쇄 미리보기

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HRID 1073094 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 stirred overnight at room temperature. The mixture is then neutralized using 10 ml of acetic acid, 1 l of water is added and the mixture is extracted with 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 removing the solvent, the residue is distilled under high vacuum.

후처리

  1. additionis added
  2. extractionthe mixture is extracted with two 500 ml portions of ether
  3. washThe combined organic phases are washed with 500 ml of saturated sodium chloride solution
  4. dry with materialdried over sodium sulphate
  5. customAfter removing the solvent
  6. distillationthe residue is distilled under high vacuum

출처 및 근거

ORD 기록
ord-851c5d54e0804b038f716259348032be
출처 데이터셋
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04968681

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