HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → (4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Bromo-4-((4-methoxybenzyl)oxy)benzaldehyde | HCID 23010223 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine | HCID 63045147 | 88% |
Reaction Steps
To a solution of 2M methylamine in MeOH (30 mL) was added intermediate 32 (2.91 g, 9.1 mmol, 1 eq). After stirring this mixture at room temperature for 30 min, the solvent was removed and the residue was partitioned between saturated NaHCO3 and DCM (2×100 mL). The organic layer was dried (Na2SO4) and concentrated. The resultant residue was dissolved in MeOH (25 mL) and, after addition of sodium borohydride (1.0 g, 27.6 mmol, 3 eq), the mixture was stirred at room temperature for 1 h. Solvent was removed and the residue was partitioned between a Na2CO3 solution and CHCl3. The resultant organic layer was dried (Na2SO4) and concentrated in vacuo to give 2.7 g, (88%) of (4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine (33).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822467B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-2e2bdbd81f0c4e6ea906aa73e3b13f53 |
| Source note | uspto-grants-2014_09 |