HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-Benzyl-5-methoxy-1,2,3,3a,8,8a-hexahydro-2-aza-cyclopenta[a]inden-8-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Benzyl-5-methoxy-2,3,3a,8a-tetrahydro-1H-2-aza-cyclopenta[a]inden-8-one | HCID 67203458 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Benzyl-5-methoxy-1,2,3,3a,8,8a-hexahydro-2-aza-cyclopenta[a]inden-8-ol | HCID 67203298 | — |
Reaction Steps
NaBH4 (0.27 g, 6.8 mmol) was added to a solution of 2-benzyl-5-methoxy-2,3,3a,8a-tetrahydro-1H-2-aza-cyclopenta[a]inden-8-one (from Example 1, Step C) (1.0 g, 3.4 mmol) in MeOH (17 mL), and stirred for 2 hours at room temperature. The reaction solution was concentrated via rotary evaporation and the residue dissolved in EtOAc. The organic solution was washed with a saturated aqueous NaHCO3 solution and brine, dried over MgSO4, and concentrated. The crude product was obtained without further purification. MS calculated for C19H21NO2+H: 296, observed: 296.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935830B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-651c98ecde5047dfa597eb3b30ae4a5f |
| Source note | uspto-grants-2011_05 |