Water → N-methyl-N-propionyl-L-alanine methyl ester

HRID 2163814ノート

反応式

HRID 2163814 の反応式
Cl.CO[C:4](=[O:9])[C@H:5]([CH3:8])NC.[C:10]([O:14][C:15](=[O:18])[CH2:16][CH3:17])(=O)CC.[CH2:19]([N:21](CC)CC)C.O>C(Cl)(Cl)Cl.C(OCC)(=O)C>[CH3:10][O:14][C:15](=[O:18])[C@H:16]([CH3:17])[N:21]([CH3:19])[C:4](=[O:9])[CH2:5][CH3:8]

参加物

7

反応物 4

HCID 962WaterHCID 8471TriethylamineHCID 31263Propionic anhydrideHCID 13850987N-Methyl-L-alanine methyl ester hydrochloride (1:1)

生成物 1

HCID 53825128N-methyl-N-propionyl-L-alanine methyl ester

試薬・触媒・溶媒 2

HCID 6212Chloroform溶媒HCID 8857Ethyl Acetate溶媒

実験手順

In 150 ml of chloroform was dissolved 28 g (0.18 mol) of N-methyl-L-alanine methyl ester hydrochloride, followed by addition of 27 g (0.21 mol) of propionic anhydride and 33 ml of triethylamine. The mixture was allowed to stand at room temperature overnight. With the addition of 100 ml of water, the reaction mixture was stirred at room temperature for 30 minutes. Thereafter, 600 ml of ethyl acetate was added and the organic layer was washed with aqueous sodium hydrogen carbonate and water in the order mentioned, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. In the above manner, N-methyl-N-propionyl-L-alanine methyl ester was obtained as a yellow oil. NMR spectrum (CDCl3) δ: 1.15(3H,t,J=7Hz), 1.40(3H,d,J=7Hz), 2.40(2H,q,J=7Hz), 2.93(3H,s), 3.70(3H,s), 5.27(1H,q, J=7Hz)

後処理

  1. washthe organic layer was washed with aqueous sodium hydrogen carbonate and water in the order
  2. dry with materialdried over anhydrous sodium sulfate
  3. customThe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-5c29aabdfa0c4027b6f87eb90a45d80e
出典データセット
uspto-grants-1979_01
特許番号
US04137230

反応ノート

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