HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258954Generated: October 30, 2026
Trimethylamine → N,N,N-Trimethyl-1-(trimethoxysilyl)ethan-1-aminium bromide
https://huagongshe.com/reaction/258954
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | HCID 21468237 | HCID 21468237 | — |
| Product | N,N,N-Trimethyl-1-(trimethoxysilyl)ethan-1-aminium bromide | HCID 21425136 | — |
Reaction Steps
One quarter mole of the alpha-bromoethyltrimethoxysilane (57.3g) is placed in an autoclave along with 17.7g of trimethylamine. The mixture is heated to 80° C. for 6 hours under 200 p.s.i. nitrogen. The excess trimethylamine is allowed to evaporate after the product has been removed from the autoclave, leaving the bromide salt of alpha-trimethylammonioethyltrimethyoxysilane bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04035411 |
|---|
| Source dataset | uspto-grants-1977_07 |
|---|
| ORD ID | ord-e6a8100ada0744b9988790595bf0ec59 |
|---|
| Source note | uspto-grants-1977_07 |
|---|
