Acetic Anhydride → N-acetyl-N-methyl-L-alanine methyl ester

HRID 1660103ノート

反応式

HRID 1660103 の反応式
Cl.[CH3:2][O:3][C:4](=[O:9])[C@H:5]([CH3:8])[NH:6][CH3:7].[C:10](OC(=O)C)(=[O:12])[CH3:11].C(N(CC)CC)C.C(=O)([O-])O.[Na+]>C(Cl)(Cl)Cl.O>[CH3:2][O:3][C:4](=[O:9])[C@H:5]([CH3:8])[N:6]([C:10](=[O:12])[CH3:11])[CH3:7]

参加物

7

反応物 4

HCID 7918Acetic Anhydride2 回HCID 8471TriethylamineHCID 516892Sodium BicarbonateHCID 13850987N-Methyl-L-alanine methyl ester hydrochloride (1:1)

生成物 1

HCID 54357781N-acetyl-N-methyl-L-alanine methyl ester

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6212Chloroform溶媒2 回

実験手順

In 300 ml of chloroform was dissolved 33.7 g (0.22 mole) of N-methyl-L-alanine methyl ester.hydrochloride, followed by the addition of 65 ml of acetic anhydride and 110 ml of triethylamine. The mixture was allowed to stand at room temperature for 24 hours and, after the excess acetic anhydride was decomposed with water, was neutralized with sodium hydrogen carbonate. The chloroform layer was separated, the water layer was extracted with ethyl acetate (120 ml×5), and the chloroform and ethyl acetate layers were combined and concentrated under reduced pressure. The brown oil thus obtained was dissolved in chloroform, washed with aqueous sodium hydrogen carbonate and concentrated under reduced pressure. By the above procedure there was obtained 31.8 g of N-acetyl-N-methyl-L-alanine methyl ester as brown oil.

後処理

  1. customThe chloroform layer was separated
  2. extractionthe water layer was extracted with ethyl acetate (120 ml×5)
  3. concentrationconcentrated under reduced pressure
  4. customThe brown oil thus obtained
  5. washwashed with aqueous sodium hydrogen carbonate
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-084927f84e3d41f3b12975bb5f3edf33
出典データセット
uspto-grants-1981_12
特許番号
US04307016

反応ノート

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