HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374255Generated: October 25, 2026
Benzylamine → N-[(Trimethylsilyl)methyl]benzylamine
https://huagongshe.com/reaction/374255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Product | N-[(Trimethylsilyl)methyl]benzylamine | HCID 353458 | — |
Reaction Steps
A mixture of chloromethyltrimethylsilane (325g, 370 ml, 2.65 mole) and benzylamine (835 g, 850 ml, 7.78 mole) was heated at 120° C. (oil bath temperature) for 2 h. A white solid began appearing after only 10 minutes and a viscous mixture eventually resulted. The reaction mixture was allowed to cool, then basified with potassium carbonate solution and extracted twice with ether. The combined extracts were dried (Na2SO4) and concentrated in vacuo to leave a yellow oil, which was purified by distillation. The excess benzylamine was removed in the first fractions (b.p. 47°-62° C. at 2 mmHg). The title compound (D10) was obtained as a colourless oil (380 g, 74%) b.p. 75°-80° C. at 2 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05166357 |
|---|
| Source dataset | uspto-grants-1992_11 |
|---|
| ORD ID | ord-c3e2d58493ae4b80a2f18d2a5f6e8769 |
|---|
| Source note | uspto-grants-1992_11 |
|---|