HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → N-(2,4-dimethoxybenzyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 2,4-Dimethoxybenzaldehyde | HCID 69175 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Toluene water | HCID 22272177 | — |
| Catalyst | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(2,4-dimethoxybenzyl)aniline | HCID 775299 | — |
Reaction Steps
Trifluoroaceticacid (10 drops) was added to a solution of 2,4-dimethoxybenzaldehyde (16.62 g, 100 mmol) and aniline (9.31 g, 100 mmol) in toluene (100 mL). The reaction mixture was stirred at reflux temperature and toluene/water was distilled off during 1.5 h. After cooling the reaction mixture was concentrated at reduced pressure and the residue was dissolved in MeOH (200 mL). NaBH4 (2.0 g, 54 mmol) was added in portions during 20 min and the reaction mixture was then stirred for 1 h. The product (22.16 g, 91%) crystallized from the reaction mixture and was isolated by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08962598B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-fb050feb02554d51be6b56241fb812d4 |
| Source note | uspto-grants-2015_02 |