Malonic Acid → (RS)-beta-Amino-beta-(4-bromophenyl)propionic acid

HRID 658138ノート

反応式

HRID 658138 の反応式
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[C:10]([OH:16])(=[O:15])[CH2:11]C(O)=O.C([O-])(=O)C.[NH4+:21]>C(O)C>[NH2:21][CH:6]([C:5]1[CH:8]=[CH:9][C:2]([Br:1])=[CH:3][CH:4]=1)[CH2:11][C:10]([OH:16])=[O:15]

参加物

5

反応物 3

HCID 867Malonic AcidHCID 707414-BromobenzaldehydeHCID 517165Ammonium Acetate

生成物 1

HCID 554034(RS)-beta-Amino-beta-(4-bromophenyl)propionic acid

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

4-Bromobenzaldehyde (50.0 g, 270 mmol), malonic acid (28.1 g, 270 mmol) and ammonium acetate (27.7 g, 359 mmol, 1.3 eq.) are dissolved in ethanol (400 ml). The mixture is heated at reflux for 16 h. The resulting solid is collected on a glass filter funnel, collected with suction filtration and washed with ethanol. The residue is then recrystallized from methanol (80 ml). It is subsequently triturated with ethyl acetate and collected by suction filtration. 41.0 g (0.16 mmol, 62% of theory) of the title compound are obtained as a colorless crystalline solid.

後処理

  1. temperatureThe mixture is heated
  2. temperatureat reflux for 16 h
  3. customThe resulting solid is collected on a glass
  4. filtrationfilter funnel
  5. filtrationcollected with suction filtration
  6. washwashed with ethanol
  7. customThe residue is then recrystallized from methanol (80 ml)
  8. customIt is subsequently triturated with ethyl acetate
  9. filtrationcollected by suction filtration

出典と根拠

ORDレコード
ord-d33f66fa40774fc9b180b6abb8e9e78a
出典データセット
uspto-grants-2011_12
特許番号
US08076285B2

反応ノート

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