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求苯胺合成苯酚的资料（急）
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求 2－甲基－6－硝基苯胺 通过重氮化水解后得 2－甲基－6－硝基苯酚的合成步骤 或者 从邻甲基苯酚 经硝化合成 2－甲基－6－硝基苯酚 的合成步骤 相关文献也可以 最好是发相关的文献给我 ylz983@126.com 非常感谢 [ Last edited by ylz83 on 2007-8-8 at 13:27 ] |
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xhz1967
金虫 (正式写手)
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- 性别: GG
- 专业: 有机分子功能材料化学
4楼2007-08-08 09:47:39
xhz1967
金虫 (正式写手)
- 应助: 19 (小学生)
- 金币: 1332.7
- 红花: 1
- 帖子: 432
- 在线: 55.5小时
- 虫号: 422897
- 注册: 2007-07-18
- 性别: GG
- 专业: 有机分子功能材料化学
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Nitration of some phenols and anilines under mild conditions. Kashmiri, M. Akram; Khan, M. Shafiq. Dep. Chem., Gov. Coll., Lahore, Pak. Science International (Lahore) (1989), 1(3), 177-9. CODEN: SINTE8 ISSN: 1013-5316. Journal written in English. CAN 112:118358 AN 1990:118358 CAPLUS Abstract Nitration of some phenols and anilines with 4-methyl-4-nitrotetrabromocyclohexadienone in ether under mild conditions is reported. Resorcinol, pyrogallol, catechol, o-cresol, o- and m-toluidines gave 4-substituted products while hydroquinone, p-cresol, p-toluidine and phloroglucinol gave 2-substituted products. Phenol and aniline both gave a mixt. of ortho and para substituted products. While benzene, toluene, anisole and N,N-diethylanaline were not nitrated under the conditions. |
2楼2007-08-08 09:37:46
xhz1967
金虫 (正式写手)
- 应助: 19 (小学生)
- 金币: 1332.7
- 红花: 1
- 帖子: 432
- 在线: 55.5小时
- 虫号: 422897
- 注册: 2007-07-18
- 性别: GG
- 专业: 有机分子功能材料化学
|
Nitration of aromatic compounds with 4-methyl-4-nitro-2,3,5,6-tetrabromocyclohexadienone under mild conditions. Kashmiri, M. Akram; Munawar, Munawar Ali; Yasmin, Rizwana; Khan, M. Shafiq. Dep. Chem., Gov. Coll., Lahore, Pak. Journal of Natural Sciences and Mathematics (1988), 28(2), 289-301. CODEN: JNSMAC ISSN: 0022-2941. Journal written in English. CAN 111:57142 AN 1989:457142 CAPLUS Abstract 4-Methyl-4-nitrotetrabromocyclohexadienone in ether was successfully used for the mononitration of highly activated arom. substances which contain hydroxy and amino groups, at room temp. For example, catechol, p-cresol, and aniline were converted into 4-nitrocatechol, 2-nitro-p-cresol, and 4-nitroaniline resp., in good yield. In the case of phenol and aniline minor quantities of o-nitro derivs. were also obtained. The results show that the reagent is very useful for the selective mononitration of arom. substrates which contain hydroxy or amine groups. Two possible mechanisms, one involving charge-transfer complex formation and another one involving ion pair formation, are proposed. |
3楼2007-08-08 09:41:05
5楼2007-08-08 13:27:31
