HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Benzyloxy-2-(4-benzyloxyphenyl)isoindoline → 5-Hydroxy-2-(4-hydroxyphenyl)isoindoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Benzyloxy-2-(4-benzyloxyphenyl)isoindoline | HCID 69472856 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5-Hydroxy-2-(4-hydroxyphenyl)isoindoline | HCID 69472920 | 42.6% |
Reaction Steps
5-Benzyloxy-2-(4-benzyloxyphenyl)isoindoline (400 mg) in TFA (12 mL) was refluxed under nitrogen atmosphere for 1 h and cooled. The solvents were removed under vacuum. The residue was dissolved in ethyl acetate (100 mL) and washed with saturated sodium bicarbonate (twice) then brine. Purification by chromatography on silica gel (eluant: dichloromethane—methanol 95:5) gave the title compound (95 mg) as a tan solid. 1H NMR (DMSO-d6): 9.35 (s, 1H), 8.53 (s, 1H), 7.14 (d, 1H, J=8.4 Hz), 6.75 (s br, 1H), 6.69 (m, 3H), 6.49 (d, 2H, J=8.7 Hz), 4.38 (m, 4H); MS: 228 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07256201B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-7290c3167f08488eb813835ec1c34f46 |
| Source note | uspto-grants-2007_08 |