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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461563Generated: October 26, 2026

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

https://huagongshe.com/reaction/1461563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,4,4,6,6,8,8-OctamethylcyclotetrasilazaneHCID 66100—
Catalyst2,2,4,4,6,6,8,8-OctamethylcyclotetrasilazaneHCID 66100—
Catalyst5-Amino-2-methylbenzenesulfonic acidHCID 67054—
Product2,2,4,4,6,6-HexamethylcyclotrisilazaneHCID 66094—

Reaction Conditions

Temperature97 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075474
Source datasetuspto-grants-1991_12
ORD IDord-ac928fd5c76e4e48b2464afae04e1d3c
Source noteuspto-grants-1991_12