HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 5,6-Dihydroimidazo[1,5-d][1,4]benzoxazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 5-(2-Hydroxyphenyl)-1H-imidazole-1-ethanol | HCID 58294136 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,6-Dihydroimidazo[1,5-d][1,4]benzoxazepine | HCID 58294110 | 84% |
Reaction Steps
To a stirred solution of 2-(1-(2-hydroxyethyl)-1H-imidazol-5-yl)phenol (103.0 mg, 0.5 mmol) and PPh3 (157.0 mg, 0.6 mmol) in THF (4 mL) at 0° C., was added DEAD (0.22 mL, 40% solution in toluene, 0.75 mmol). The resulting yellow solution was allowed to warm to rt and stirred overnight. The solvent was removed under reduced pressure and the crude residue was purified by flash column chromatography on silica gel to afford the desired product in 84% yield. 1H NMR: 4.35-4.45 (m, 4H), 6.94-7.05 (m, 2H), 7.11-7.19 (m, 1H), 7.43 (d, 1H, J=0.8 Hz), 7.49 (s, 1H), 7.67 (dd, 1H, J=1.6, 8.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748469B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-b5afb2c1b9e847f791564d107c9f3382 |
| Source note | uspto-grants-2014_06 |