1)  o-Toluenesulfonyl chloride
邻甲苯磺酰氯
2)  o-Toluene sulfochloride
邻甲苯磺酰氯
3)  2-Toluenesulfonyl chloride
邻甲苯磺酰氯
4)  o-toluene sulfonyl chloride
邻甲苯磺酰氯
5)  o-methylaniline
邻甲苯胺
1.
3-Methyl-4-acetaminobenzenesulfonyl chloride(Ⅰ) was prepared from o-methylaniline by protecting the amino group and then reacting with chlorosulfonic acid.
合成步骤如下:(1)邻甲苯胺、对甲氧基苯胺的氨基保护后,分别与氯磺酸反应得3-甲基-4-乙酰氨基苯磺酰氯(Ⅰ)和2-甲氧基-5-乙酰氨基苯磺酰氯(Ⅴ);(2)对氨基乙酰苯胺(Ⅱ)分别与Ⅰ、Ⅴ在w(CH3COOH)=5%的醋酸中反应,所得缩合物水解得产品Ⅳ、Ⅶ。
2.
o-Fluorobenzoic acid was synthesized by Schiemann-reaction of o-methylaniline to give o-fluorotoluene which was oxidized by HNO 3 in an autoclave to abtain the product of 70.
以邻甲苯胺为原料 ,经西曼反应合成邻氟甲苯 ,进而经硝酸氧化法得到邻氟苯甲酸 (收率 93。
6)  o-methyl
邻甲基
1.
Two series of sulfonated poly(ether ether ketone)s based on tert-butylhydroquione and o-methylhydroquione were synthesized via aromatic nucleophilic substitution reaction.
以特丁基对苯二酚和邻甲基对苯二酚分别制备两个系列磺化聚醚醚酮。
参考词条
补充资料:邻甲苯磺酰氯
分子式:C7H7ClO2S
分子量:190.65
CAS号:133-59-5

性质:油状液体。熔点10.2℃,沸点154℃(4.8kPa),126℃(1.33kPa),相对密度1.3383(20/4℃),折光率1.5565。溶于热醇、醚、苯,不溶于水。

制备方法:由甲苯氯磺化而得。

用途:用于有机合成和糖精生产。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。