中试规模合成邻硝基苯乙醇  

Scale-up Synthesis of o-Nitrophenylethanol

作　　者：郭翔海[1] 彭志亮[1] 郑双江[1] 沈家祥[1] 

机构地区：[1]天津大学药物科学与技术学院,天津300072

出　　处：《精细化工》2008年第1期98-101,共4页Fine Chemicals

摘　　要：该文研究了重要中间体邻硝基苯乙醇的合成工艺。结果表明,对于邻硝基甲苯的羟甲基化反应,效果最好的催化剂为氢氧化钠水溶液,且质量分数为20%的氢氧化钠水溶液的催化效果最佳,强碱型阴离子交换树脂因溶于二甲亚砜不适用于该反应。在质量分数20%的氢氧化钠水溶液催化下,羟甲基化反应最佳反应温度为50℃,甲醛与邻硝基甲苯的最佳摩尔比为0.4-0.5。在该条件下,按已转化的邻硝基甲苯计,邻硝基苯乙醇质量收率为110%,摩尔收率为90.7%。产品邻硝基苯乙醇的结构经红外、核磁等表征确证。该实验结果已经经过一次性投邻硝基甲苯120 kg的生产型中试验证,邻硝基苯乙醇质量收率为105.2%,摩尔收率为86.7%。The synthetic process of important intermediate o-nitrophenylethanol was studied. Results showed that, with w （NaOH） = 20% aqueous solution as alkaline catalyst, at a temperature of 50℃ and formaldehyde to o-nitrotoluene molar ratio of 0. 4 - 0. 5, best result was obtained. Under these optimized conditions,taking account of recovered o-nitrotoluene, o-nitrophenylethanol was afforded in mass yield of 110% and molar yield of 90. 7%. The product was confirmed by IR and 1H,^13CNMR. The result of our experiments was proved by productive scale-up test,in which 120 kg o-nitrotoluene was used as raw material to afford o-nitrophenylethanol in a mass yield of 105.2% and a molar yield of 86.7%.

关 键 词：邻硝基苯乙醇 邻硝基甲苯 羟甲基化 吲哚合成 精细化工中间体 

分 类 号：TQ612[化学工程—精细化工]