Triethylamine → N-(2-chloro-6-nitrobenzyl)-L-alanine ethyl ester

HRID 127571

反応式

HRID 127571 の反応式
Cl.[CH2:2]([O:4][C:5](=[O:9])[C@H:6]([CH3:8])[NH2:7])[CH3:3].C(N(CC)CC)C.Br[CH2:18][C:19]1[C:24]([N+:25]([O-:27])=[O:26])=[CH:23][CH:22]=[CH:21][C:20]=1[Cl:28]>C(O)C>[CH2:2]([O:4][C:5](=[O:9])[C@H:6]([CH3:8])[NH:7][CH2:18][C:19]1[C:24]([N+:25]([O-:27])=[O:26])=[CH:23][CH:22]=[CH:21][C:20]=1[Cl:28])[CH3:3]

参加物

5

反応条件

温度
80 °C

実験手順

18.24 g of L-alanine ethyl ester hydrochloride in 60 ml of ethanol was added dropwise to a mixture of 25 ml of triethylamine in 60 ml of ethanol and the mixture was heated to 80° C. The resulting solution was added dropwise at this temperature to a solution of 15 g of α-bromo-2-chloro-6-nitrotoluene in 60 ml of ethanol. The mixture was stirred at 80° C. overnight and then evaporated to dryness. The residue was treated with 150 ml of deionised water and extracted twice with 100 ml of methylene chloride. The methylene chloride extracts were washed with water, dried and evaporated. The resulting product was purified by chromatography on silica gel with methylene chloride/5% methanol. There were obtained 15.75 g (91% of theory) of N-(2-chloro-6-nitrobenzyl)-L-alanine ethyl ester; nD20 =1.5267.

後処理

  1. customevaporated to dryness
  2. additionThe residue was treated with 150 ml of deionised water
  3. extractionextracted twice with 100 ml of methylene chloride
  4. washThe methylene chloride extracts were washed with water
  5. customdried
  6. customevaporated
  7. customThe resulting product was purified by chromatography on silica gel with methylene chloride/5% methanol

出典と根拠

ORDレコード
ord-b36b9db07ec04c54a12306153c9f1ab9
出典データセット
uspto-grants-1981_03
特許番号
US04256748

関連ノート

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