HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4,6-Trimethylaniline → HCID 24881570, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4,6-Trimethylaniline | HCID 6913 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 2,6-Difluoroaniline | HCID 79647 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Product | HCID 24881570 | HCID 24881570 | 65% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
Acetic acid (0.086 mL, 1.5 mmol) was added to a round bottom flask charged with 2,6-difluoroaniline (3 mL, 30 mmol) and triethyl orthoformate (5 mL, 30 mmol). A vigreux column was attached and the solution was heated with stirring to 120° C. for 2 hours. 2,4,6-trimethylaniline (4.22 mL, 30 mmol) was then added to the reaction mixture. The solution was heated to reflux for an additional 2 hours and cooled to room temperature, whereupon crude product precipitated. Trituration with cold hexanes and vacuum filtration provided pure N-(2,6-difluorophenyl)-N′(mesityl)-formamidine (5.35 g, 65%) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08703965B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-c1f1648a07864b3fb66d107247121cc1 |
| Source note | uspto-grants-2014_04 |