HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236424Generated: October 30, 2026
Hexamethyldisilazane → Hexamethyldisilazane
https://huagongshe.com/reaction/236424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Hexamethyldisilazane | HCID 13838 | — |
| Product | Sodium amide | HCID 24533 | — |
| Product | Sodium bis(trimethylsilyl)amide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04644076 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-21ffdfdd15734c3ea56443603e78848e |
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| Source note | uspto-grants-1987_02 |
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