HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → (1-Benzofuran-2-ylmethyl)(methyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-Benzofurancarboxaldehyde | HCID 61341 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1-Benzofuran-2-ylmethyl)(methyl)amine | HCID 5048607 | 50.2% |
Reaction Steps
To a stirred solution of 2-benzofurancarboxaldehyde (2.22 g, 15.2 mmole) in MeOH (5 mL) was added 2 M methylamine in MeOH (15 mL), HOAc (0.86 mL, 15 mmole), and NaBH3CN (1.0 g, 15.9 mmole). The reaction was stirred for 18 h at RT then concentrated under vacuum. The remaining residue was taken up in Et2O, and the solution was washed with 1 N NaOH then brine, dried (Na2SO4), and concentrated to dryness. Purification by flash chromatography on silica gel (5% (5% NH4OH in MeOH)/CHCl3) gave the title compound (1.23 g, 50%) as a pale yellow oil: MS (ES) m/e 162.4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250424B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-ecbb58f9fc844d17911fbadbb4254d4a |
| Source note | uspto-grants-2007_07 |