HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzylamine → (4-Methoxy-benzyl)-(3-trifluoromethyl-pyridin-2-yl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Chloro-3-(trifluoromethyl)pyridine | HCID 589833 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | (4-Methoxy-benzyl)-(3-trifluoromethyl-pyridin-2-yl)-amine | HCID 29558569 | 83.1% |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
A mixture of 2-chloro-3-trifluoromethylpyridine (64.83 g, 357 mmol), 4-methoxybenzylamine (56 mL, 429 mmol) and DIPEA (73.4 mL, 429 mmol) in n-butanol (100 mL) was refluxed (oil bath temp. 140° C.) for 3.5 days. Concentrated in vacuum, partitioned between 25% HCl and TBME, reextracted the organic layer twice with 25% HCl, the aqueous layer was made alkaline with 32% NaOH, extracted with TBME, washed with brine and dried over Na2SO4. Removal of the solvent in vacuum left a brown oil (105.21 g, 104%). Vacuum distillation gave the title compound as a colorless liquid (83.766 g, 83%, 4877-2/2; bp 139-141° C. at 1.4 mbar). MS (ISP) 283.3 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504404B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-8dc84b303dea4be3bbc47a0339a56ff2 |
| Source note | uspto-grants-2009_03 |