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HRID 1461563作成日:2026年10月27日

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

https://huagongshe.com/reaction/1461563

反応式

関与物質

役割名称HCID仕込み量
反応物2,2,4,4,6,6,8,8-OctamethylcyclotetrasilazaneHCID 66100—
触媒2,2,4,4,6,6,8,8-OctamethylcyclotetrasilazaneHCID 66100—
触媒5-Amino-2-methylbenzenesulfonic acidHCID 67054—
生成物2,2,4,4,6,6-HexamethylcyclotrisilazaneHCID 66094—

反応条件

温度97 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05075474
出典データセットuspto-grants-1991_12
ORD IDord-ac928fd5c76e4e48b2464afae04e1d3c
出典メモuspto-grants-1991_12