HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-trimethylsilyl-2,6-dichloro-3-methylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | 2,6-Dichloro-3-methylaniline | HCID 116529 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-trimethylsilyl-2,6-dichloro-3-methylaniline | HCID 11128643 | 73.6% |
Reaction Steps
A solution of 50 ml of benzene, 4.0 g (22.7 mmole) of 2,6-dichloro-3-methylaniline, 10.67 ml (80.8 mmole) of trimethylsilyl bromide, and 13.1 ml (94.0 mmole) of triethylamine was heated at reflux over 42 hours. The product was isolated as described in Example 1 to provide 4.14 g (16.7 mmole, 73.5 percent yield) of 98.0 percent pure N-trimethylsilyl-2,6-dichloro-3-methylaniline as a light yellow oil, b.p. 64°-68° C. at 0.03 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04910306 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-ac2053fed34048bf849b87c13384a95b |
| Source note | uspto-grants-1990_03 |