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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236424Generated: October 30, 2026

Hexamethyldisilazane → Hexamethyldisilazane

https://huagongshe.com/reaction/236424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethyldisilazaneHCID 13838—
ReactantSodium amideHCID 24533—
ReactantAmmonium ChlorideHCID 25517—
SolventBenzeneHCID 241—
ProductHexamethyldisilazaneHCID 13838—
ProductSodium amideHCID 24533—
ProductSodium bis(trimethylsilyl)amideHCID 2724254—

Reaction Steps

The chemistry of the final HMDS filtrate treatment step is complex. The reactions occurring in the final amide treatment and distillation steps are, however, not fully understood. Thus, the following description should be understood as presently incomplete and partly hypothetical. In liquid anhydrous ammonia, sodium amide reacts rapidly with ammonium chloride to form ammonia and sodium chloride according to the formula: ##STR1## This reaction proceeds slowly, if at all, in HMDS. The ammonium chloride appears to react with a reaction product formed when crude HMDS is "treated" with sodium amide. In this regard, literature reports that sodium bis(trimethylsilyl)amide is formed from the reaction of sodium amide and HMDS in benzene as follows: ##STR2## This reaction proceeds moderately at 25°-30° C. with evolution of ammonia without benzene as a solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04644076
Source datasetuspto-grants-1987_02
ORD IDord-21ffdfdd15734c3ea56443603e78848e
Source noteuspto-grants-1987_02