HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-(azepan-1-yl)-N-benzyl-N-methylpropan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(Azepan-1-yl)propan-1-amine | HCID 2764395 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(azepan-1-yl)-N-benzyl-N-methylpropan-1-amine | HCID 58540516 | — |
Reaction Steps
To a mixture of 3-(Azepan-1-yl)propan-1-amine (0.10 g, 0.64 mmole) in methylene chloride (5 mL) were added benzaldehyde (0.64 mmole) and NaBH(OAc)3 (0.63 g, 3.0 mmol). The reaction solution was stirred at room temperature for 3 h. Then, paraformaldehyde (200 mg) was added to the reaction mixture and stirring was continued for 6 h. 2N aqueous NaOH (2 mL) was added to quench the reaction, followed by addition of methylene chloride (30 mL). The organic layer was separated, dried over anhydrous Na2SO4, and filtered. The filtrate was evaporated to supply 3-(azepan-1-yl)-N-benzyl-N-methylpropan-1-amine (151 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08729081B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-f21b74ff1a3e4dc2a06628c956941480 |
| Source note | uspto-grants-2014_05 |