Methanol → 4-Amino-L-phenylalanine methyl ester

HRID 36126ノート

反応式

HRID 36126 の反応式
[NH2:1][C:2]1[CH:13]=[CH:12][C:5]([CH2:6][C@@H:7]([C:9]([OH:11])=[O:10])[NH2:8])=[CH:4][CH:3]=1.S(Cl)(Cl)=O.[CH3:18]O>C(OCC)(=O)C>[CH3:18][O:10][C:9](=[O:11])[C@H:7]([CH2:6][C:5]1[CH:4]=[CH:3][C:2]([NH2:1])=[CH:13][CH:12]=1)[NH2:8]

参加物

5

反応物 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 1510014-Aminophenylalanine

生成物 1

HCID 206108304-Amino-L-phenylalanine methyl ester収率 88.5%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

To a stirred solution of p-aminophenylalanine (2.05 g, 9.9 mmol) in methanol (100 ml) at 0° C. was added thionyl chloride (20 ml) dropwise. Upon complete addition the reaction mixture was heated under reflux. After 24 hours the reaction mixture was cooled and reduced under pressure to give a brown oil. The brown oil was taken up in ethyl acetate (200 ml) and washed with saturated sodium bicarbonate solution (200 ml). The aqueous layer was further extracted with ethyl acetate (5×200 ml). The combined organic layer was dried over MgSO4 and reduced under pressure to yield the title compound as a brown solid (1.7 g, 88.5%).

後処理

  1. additionUpon complete addition the reaction mixture
  2. temperaturewas heated
  3. temperatureunder reflux
  4. temperatureAfter 24 hours the reaction mixture was cooled
  5. customto give a brown oil
  6. washwashed with saturated sodium bicarbonate solution (200 ml)
  7. extractionThe aqueous layer was further extracted with ethyl acetate (5×200 ml)
  8. dry with materialThe combined organic layer was dried over MgSO4

出典と根拠

ORDレコード
ord-8532da8425fd4449b98d17aac0460488
出典データセット
uspto-grants-1995_05
特許番号
US05412145

反応ノート

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