HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → Benzyl-(2-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2-Methoxy-8,9-dihydro-5H-benzo[7]annulen-6(7H)-one | HCID 12369177 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Acetic acid methanol | HCID 10129899 | — |
| Product | Benzyl-(2-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)-amine | HCID 18007141 | 83.2% |
Reaction Steps
Dissolve 2-Methoxy-5,7,8,9-tetrahydro-benzocyclohepten-6-one (prepared according to JCS Perkin Trans. 1, 1992, 1475-1481, 83 mg, 0.44 mmol) in 1 mL of 19:1 methanol/acetic acid as solvent, and treat the solution with benzylamine (60 uL, 65 mg, 0.60 mmol) and NaCNBH3 (80 mg, 1.27 mmol). Agitate the reaction mixture overnight, then dilute with 25 mL dichloromethane. Wash the organic layer with 25 mL 10% aqueous potassium carbonate solution, the 25 mL brine, dry over MgSO4 and evaporate to yield 103 mg product, used in subsequent chemistry without further purification; 80% crude yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07399774B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-3568d788e3844f408d6af9ef6cfa6705 |
| Source note | uspto-grants-2008_07 |