HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → [5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-ylmethyl]-methyl-phenethyl-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-Methylbenzeneethanamine | HCID 11503 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(4-Bromo-phenyl)-3-methyl-isoxazole-4-carbaldehyde | HCID 82133792 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-ylmethyl]-methyl-phenethyl-amine | HCID 66577314 | — |
Reaction Steps
5-(4-Bromo-phenyl)-3-methyl-isoxazole-4-carbaldehyde (0.150 g, 0.56 mmol) and N-methyl-phenethyl-amine (0.10 mL, 0.67 mmol) were combined in MeOH and stirred at room temperature overnight. Once no starting material was seen by analytical LCMS, sodium borohydride (0.064 g, 1.69 mmol) was added and the reaction was stirred at room temperature for 1 hour. H2O was added and the mixture was extracted with EtOAc. The combined organic layers were dried and concentrated, and the residue was purified by silica gel chromatography to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09090573B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-04eeffc8b4d24d33a8222decffa51435 |
| Source note | uspto-grants-2015_07 |