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

HRID 704743
ノート
印刷プレビュー

反応式

HRID 704743 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 887Methanol溶媒
HCID 962
Water
溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-9773d333a19e499ca576a1866e57fa31
出典データセット
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04988711

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート