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机构地区:[1]常熟理工学院化学与材料工程系,常熟215500 [2]常熟市湖滨化工有限公司
出 处:《石油炼制与化工》2007年第12期28-32,共5页Petroleum Processing and Petrochemicals
基 金:江苏省高校自然科学研究课题基金资助项目(05KJD150002);江苏省新型功能材料重点建设实验室开放研究课题基金资助项目(05KFJJ001)
摘 要:介绍了以二环戊基二氯硅烷(DCPDCS)为中间产物合成二环戊基二甲氧基硅烷(DCPDMS)的方法。首先通过研究得到了合成DCPDCS的最佳工艺条件,即反应压力1.0~1.2MPa,n(二氯硅烷)/n(环戊烯)=1.16,反应温度85~95℃,催化剂用量1.2g,异辛醇用量2.3g,反应时间6~7h。在该条件下环戊烯转化率可达96%以上,DCPDCS收率可达88%以上。DCPDMS的合成条件为:第一阶段n(甲醇)/n(DCPDCS)=1.33,反应温度为室温;第二阶段n(甲醇)/n(DCPDCS)=4.95,反应温度低于50℃。在该条件下DCPDCS转化率为87.6%,DCPDMS收率为79.5%。Dicyclopentyldimethoxysilane(DCPDMS) was synthesized by the addition of silicon hydride method and the reaction conditions were studied. Firstly,dicyclopentyldichlorosilane(DCPDCS), a reaction intermediate,was prepared under the optimal conditions of a reaction pressure range of 1.0- 1.2 MPa, a n (dichlorosilane)/n (cyclopentene)of 1. 16, a reaction temperature range of 85-95℃, a catalyst dosage of 1.2 g,an isooctyl alcohol dosage of 2.3 g and a reaction time range of 6-7 h. The conversion of cyclopentene and the yield of DCPDCS were 96. 2% and 88. 9%, respectively. Then DCPDMS was synthesized under the following reaction conditions: in the first reaction stage and the second reaction stage, the n (methanol)/n (DCPDCS) was 1. 33 and 4. 95, respectively; the reaction temperature was ambient temperature and below 50 ℃ ,respectively. The conversion of DCPDCS reached 87.6%,and the DCPDMS yield was 79.5%.
关 键 词:二环戊基二甲氧基硅烷 二环戊基二氯硅烷 加成反应 合成
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