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.[Cl:17][C:18]1[CH:25]=[CH:24][CH:23]=[C:22]([N+:26]([O-:28])=[O:27])[C:19]=1[CH2:20]Br>C(O)C>[CH2:2]([O:4][C:5](=[O:9])[C@@H:6]([CH3:8])[NH:7][CH2:20][C:19]1[C:22]([N+:26]([O-:28])=[O:27])=[CH:23][CH:24]=[CH:25][C:18]=1[Cl:17])[CH3:3]参加物
反応条件
- 温度
- 80 °C
実験手順
A mixture of 18.24 g of D-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 resulting mixture was heated to 80° C. The solution obtained was added dropwise at this temperature to a solution of 15 g of 2-chloro-6-nitrobenzyl bromide 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 over sodium sulphate and evaporated. The resulting product was purified by chromatography on silica gel with methylene chloride/5% methanol. There were obtained 16 g (93% of theory) of N-(2-chloro-6-nitrobenzyl)-D-alanine ethyl ester; nD25 =1.5247; [α]D =-6.9° (c=1% in ethanol).
後処理
- customThe solution obtained
- customevaporated to dryness
- additionThe residue was treated with 150 ml of deionised water
- extractionextracted twice with 100 ml of methylene chloride
- washThe methylene chloride extracts were washed with water
- dry with materialdried over sodium sulphate
- customevaporated
- 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-8f3631eba64e4d3b959b52004ebbed82
- 出典データセット
- uspto-grants-1981_03
- 特許番号
- US04256748
関連ノート
読み込み中…