![烷基芳基化合物的制备方法](/CN/2004/8/7/images/200480037813.jpg)
基本信息:
- 专利标题: 烷基芳基化合物的制备方法
- 专利标题(英):Method for producing alkylaryl compounds
- 申请号:CN200480037813.2 申请日:2004-12-17
- 公开(公告)号:CN1997611A 公开(公告)日:2007-07-11
- 发明人: N·博特克 , J·特罗皮施 , T·纳贝舒伯 , J·斯特凡 , M·勒佩尔 , T·海德曼 , U·施泰因布伦纳 , R·本福尔
- 申请人: 巴斯福股份公司
- 申请人地址: 德国路德维希港
- 专利权人: 巴斯福股份公司
- 当前专利权人: 巴斯福股份公司
- 当前专利权人地址: 德国路德维希港
- 代理机构: 北京市中咨律师事务所
- 代理人: 林柏楠; 刘金辉
- 优先权: 10360026.4 2003.12.19 DE
- 国际申请: PCT/EP2004/014444 2004.12.17
- 国际公布: WO2005/061447 DE 2005.07.07
- 进入国家日期: 2006-06-19
- 主分类号: C07C2/66
- IPC分类号: C07C2/66 ; C07C303/06 ; C11D1/22 ; C11D11/04
The production of alkylaryl compounds comprises the following stages: a) reaction of a C4/C5 olefin mixture on a metathesis catalyst to produce a C4-8 olefin mixture containing 2-pentene and the optional isolation of the C4-8 olefin mixture; b) isolation of between 5 and 100 % of the 2-pentene obtained in step a) and subsequent reaction on an isomerisation catalyst to form a mixture of 2-pentene and 1-pentene, which is returned to stage a); c) dimerisation of the C4-8 olefin mixture obtained in stage b) after the isolation process, to form a mixture containing C8-16 olefins, isolation of the C8-16 olefins and optional isolation of a partial stream of the latter; d) reaction of the C8-16 olefin mixtures obtained in stage c) or the partial stream with an aromatic hydrocarbon in the presence of an alkylation catalyst, to form alkyl aromatic compounds, whereby prior to the reaction an additional 0 to 60 wt. % linear olefins, in relation to the C8-16 olefin mixtures obtained in stage c), can be added; e) optional sulphonation of the alkyl aromatic compounds obtained in stage d) and neutralisation to form alkylaryl sulphonates, whereby prior to the sulphonation an additional 0 to 60 wt. % linear alkyl benzols, in relation to the alkyl aromatic compounds obtained in stage d), can be added, provided that there were no admixtures in stage d); f) optional mixing of the alkylaryl sulphonates obtained in stage e) with between 0 and 60 wt. %, linear alkylaryl sulphonates, in relation to the alkylaryl sulphonates obtained in stage e), provided that there were no admixtures in stages d) and e).