HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Hydroxyphenyl)-5-benzofurancarboxylic acid → HCID 10192749, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Hydroxyphenyl)-5-benzofurancarboxylic acid | HCID 22221619 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10192749 | HCID 10192749 | 37% |
Reaction Steps
Compound 143 (0.21 g, 0.83 mmol) in THF (10 ml) was treated with BH3 THF (4.0 ml of 1.0 M) and the reaction was heated to reflux. After 2 hr, the reaction was cooled and then poured into 2NHCl and extracted with EtOAc. The organic layer was dried, concentrated and the product was purified by cloumn chromatography (60% EtOAc/Hexane) to give 144 as a solid (0.07 g, 37%); Mp=248–250° C.; 1H NMR (DMSO-d6) δ 9.86 (br s, 1 H), 7.72 (d, 2 H, J=8.3 Hz), 7.52–7.49 (m, 2 H), 7.19 (dd, 1 H, J=8.3 Hz, 1.6 Hz), 7.15 (s, 1 H), 6.87 (d, 2 H, J=8.8 Hz), 5.19 (t, 1 H, J=5.2 Hz), 4.56 (d, 2 H, J=4.1 Hz); MS 239 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022733B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-fdf7a05dbb194648b2c70f192899c877 |
| Source note | uspto-grants-2006_04 |