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(S)-吲哚啉-2-甲酸的合成工艺

Synthesis process of (S)-indoline-2-carboxylic acid
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摘要 研究(S)-吲哚啉-2-甲酸的合成工艺,以草酸二乙酯和邻硝基甲苯为起始原料,在乙醇钾作用下生成邻硝基苯丙酮酸乙酯,用雷尼镍催化加氢、镁粉还原、手性分离得目标产物(S)-吲哚啉-2-甲酸,总收率为38%(以邻硝基甲苯计算).该合成工艺成本低、环境污染小. Synthesis process of (S)-indoline-2-carboxylic acid was investigated, where diethyl oxalate and o-nitrotoluene were taken raw material to generate an intermediate the ethyl o-nitrophenylpyruvate under the action of thonotic potassium. The target product (S)-indoline-2-carboxylic acid was obtained from ethyl o-nitrophenylpyruvate by nickel-catalytic hydrogenation, magnesium powder, and reduction chiral separation. The overall yield is 38%(based on-nitrotoluene). This synthesis process is low cost and environmental pollution.
出处 《兰州理工大学学报》 CAS 北大核心 2015年第4期76-78,共3页 Journal of Lanzhou University of Technology
基金 创新团队建设计划(1207TTCA009) 国际科技合作专项(1204WCGA020)
关键词 吲哚啉-2-甲酸 合成 手性分离 indoline-2-carboxylic acid synthesis chiral separation
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