Methanol → 3-(4-Methoxyphenyl)-1-phenylprop-2-en-1-one

HRID 2101224

反応式

HRID 2101224 の反応式
[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)(=[O:3])[CH3:2].[OH-].[Na+].CO.[CH:14](=O)[C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1>C(OC(=O)C)C>[CH3:22][O:21][C:18]1[CH:19]=[CH:20][C:15]([CH:14]=[CH:2][C:1]([C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)=[O:3])=[CH:16][CH:17]=1

参加物

6

反応物 4

HCID 887MethanolHCID 7410AcetophenoneHCID 14798Sodium HydroxideHCID 312444-Methoxybenzaldehyde

生成物 1

HCID 941973-(4-Methoxyphenyl)-1-phenylprop-2-en-1-one

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

Acetophenone (0.5 g) and sodium hydroxide (0.17 g) were suspended in 15 Ml of methanol pre-chilled at −10° C. p-Anisaldehyde (0.57 g) was added thereto, and stirred for 10 hr at room temperature. After neutralization with 5% hydrochloric acid solution, the product was extracted with 100 Ml of ethylacetate. The extracted organic phase was dried with anhydrous magnesium sulfate, and concentrated under vacuum evaporator. Purified compound was obtained by elution with n-hexane:ethylacetate (v/v, 1:7) through silica gel column chromatography (5×3 cm, Merk), and identified as follows:

後処理

  1. additionwas added
  2. extractionAfter neutralization with 5% hydrochloric acid solution, the product was extracted with 100 Ml of ethylacetate
  3. dry with materialThe extracted organic phase was dried with anhydrous magnesium sulfate
  4. concentrationconcentrated under vacuum evaporator
  5. customPurified compound was obtained by elution with n-hexane

出典と根拠

ORDレコード
ord-6be23af2371049c49a375372ad07cdd3
出典データセット
uspto-grants-2009_08
特許番号
US07572831B2

関連ノート

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