HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → HCID 22396944, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethylacetate heptane | HCID 21899848 | — |
| Reactant | HCID 22396758 | HCID 22396758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22396944 | HCID 22396944 | 71% |
Reaction Steps
A solution of lithium aluminum hydride (0.17 g, 4.45 mmol) in tetrahydrofuran (3.0 mL) and a solution of 3-benzoyl-9-phenyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (0.17 g, 0.46 mmol) in tetrahydrofuran (5.0 mL) at 0° C. were reacted in a manner similar to Example 1 to give an oil. Column chromatography (silica gel, 10-50% EtOAc/heptane) afforded 0.113 g (71%) of the title compound as an oil. 1H NMR (300 MHz, CDCl3) δ 8.05, 7.66-7.57, 7.49, 7.45-7.30, 7.13-7.04, 3.98, 3.18-2.97; MS (EI) m/z 366 (M+); HRMS (FAB) calcd for C25H24N2+H: 353.2018, found: 353.2021.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06583135B2 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-6fe7c701da954245b7892756e7771122 |
| Source note | uspto-grants-2003_06 |