HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,6-Dichloro-N-trimethylsilylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,6-Dichloroaniline | HCID 11846 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2,6-Dichloro-N-trimethylsilylaniline | HCID 14362679 | 75.1% |
Reaction Steps
A solution of 60 ml of benzene, 5.0 g (30.9 mmole) of 2,6-dichloroaniline, 10.6 ml (76.0 mmole) of triethylamine, and 8.08 ml (61.1 mmole) of trimethylsilyl bromide was heated at reflux for 54 hours, cooled, filtered, and the solvent was removed from the filtrate in vacuo. The residue was evacuated at 1 mm to remove any excess trimethylsilyl bromide. The residual mixture was filtered into a round-bottomed flask and distilled using a short Vigreaux column to provide 5.43 g (23.2 mmole, 75.0 percent yield) of the N-trimethylsilyl-2,6-dichloroaniline as a 97 percent pure amber oil, bp 74° C.-75° C. at 0.4 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04910306 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-ce9fdf01c75b4c6fb2f6d34b35bd44d1 |
| Source note | uspto-grants-1990_03 |