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Water → HCID 53730131、化合物

HRID 746022
ノート
印刷プレビュー

反応式

HRID 746022 の反応式
C(=O)([O-])O.[Na+].Cl.[NH2:7][CH:8]([C:13](=[O:16])[CH2:14][CH3:15])[C:9]([O:11][CH3:12])=[O:10].O.[C:18](Cl)(=[O:27])[CH:19]=[CH:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>C(OCC)(=O)C>[C:18]([NH:7][CH:8]([C:13](=[O:16])[CH2:14][CH3:15])[C:9]([O:11][CH3:12])=[O:10])(=[O:27])[CH:19]=[CH:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 660233-Phenylprop-2-enoyl chlorideHCID 516892Sodium BicarbonateHCID 23311259HCID 23311259、化合物

生成物 1

HCID 53730131HCID 53730131、化合物

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒2 回

実験手順

Sodium hydrogen carbonate (10.0 g) was added to a mixture of methyl 2-amino-3-oxovalerate hydrochloride (9.1 g), ethyl acetate (50 ml) and water (40 ml) with ice-cooling and stirring followed by dropwise addition of a solution of cinnamoyl chloride (8.3 g) in ethyl acetate (10 ml). The whole mixture was stirred under ice-cooling for 2 hours and the ethyl acetate layer was separated. The aqueous layer was extracted with ethyl acetate. The ethyl acetate layers were combined, washed with water and dried over anhydrous magnesium sulfate. The solvent was then distilled off and isopropyl ether was added to the residue to give methyl 2-cinnamoylamino-3-oxovalerate as crystals; yield 8.8 g (63.8%). Recrystallization from ethanol gave colorless needles melting at 119°-120° C.

後処理

  1. temperaturecooling
  2. stirringThe whole mixture was stirred under ice-
  3. temperaturecooling for 2 hours
  4. customthe ethyl acetate layer was separated
  5. extractionThe aqueous layer was extracted with ethyl acetate
  6. washwashed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. distillationThe solvent was then distilled off
  9. additionisopropyl ether was added to the residue

出典と根拠

ORDレコード
ord-31414afa27f5402da0638b94b780e102
出典データセット
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04602027

反応ノート

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