HuagongsheHuagongshe Chemistry Print Report · For research reference only
5,6,11,12-Tetrahydrodibenz[b,f]azocin-6-one → 5,6,11,12-Tetrahydrodibenzo[b,f]azocine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5,6,11,12-Tetrahydrodibenz[b,f]azocin-6-one | HCID 80146 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,6,11,12-Tetrahydrodibenzo[b,f]azocine | HCID 610577 | 72% |
Reaction Steps
To a suspension of 11,12-dihydro-5H-dibenzo[b,f]azocin-6-one (2.0 g, 8.96 mmol) in dry THF (20 ml) is added dropwise a solution of LiAlH4 (1.0 N in THF, 8.96 ml) over a period of 10 min. After ceasing of gas evolution, the reaction mixture is kept stirring at reflux overnight, then quenched by the addition of water (0.48 ml). The precipitate is filtered off and the filtrate is extracted twice with EtOAc. The combined organic layers are dried over Na2SO4, the solvent is evaporated and the residue recrystallized from boiling hexane to give off white crystals of the title compound (1.35 g) in 72% yield: tR (LC-2) 1.65 min; ESI-MS(+): m/z 210.70 [M+H]+ (calcd 209.29 for C15H15N).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897788B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-ffb5ce934f784021b5353f7493e157f7 |
| Source note | uspto-grants-2011_03 |