돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1461563생성일: 2026년 10월 26일

2,2,4,4,6,6,8,8-Octamethylcyclotetrasilazane → 2,2,4,4,6,6-Hexamethylcyclotrisilazane

https://huagongshe.com/reaction/1461563

반응식

참여 물질

역할이름HCID투입량
반응물2,2,4,4,6,6,8,8-OctamethylcyclotetrasilazaneHCID 66100—
촉매2,2,4,4,6,6,8,8-OctamethylcyclotetrasilazaneHCID 66100—
촉매5-Amino-2-methylbenzenesulfonic acidHCID 67054—
생성물2,2,4,4,6,6-HexamethylcyclotrisilazaneHCID 66094—

반응 조건

온도97 °C

반응 단계

A 200 ml volume glass flask equipped with a stirring machine, a condenser, a distillation column and a tube for distilling off the resulting product was provided. 73 g of octamethyl cyclotetrasilazane and 3.65 g of p-toluidine-m-sulfonic acid as a catalyst were introduced into the glass flask and the content of the flask was heated to 97° C. The content of the flask was stirred after it was confirmed that the octamethyl cyclotetrasilazane was completely molten. When the internal pressure of the reaction system was reduced to 65 torr with a vacuum pump to obtain a distillate, 68 g of hexamethyl cyclotrisilazane was obtained through the distillation over one hour. The resulting hexamethyl cyclotrisilazane had a high purity in the order of 99.1 GC % and the yield thereof was 93.2%. Thus, highly pure hexamethyl cyclotrisilazane could be obtained at a high yield within a short period of time. Moreover, almost no high boiling point substance remained in the reaction system.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05075474
출처 데이터셋uspto-grants-1991_12
ORD IDord-ac928fd5c76e4e48b2464afae04e1d3c
출처 메모uspto-grants-1991_12