HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 136078943, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 56959336 | HCID 56959336 | — |
| Reactant | 4-(6-Hydroxyquinolin-2-yl)-3-methoxybenzoic acid | HCID 56961057 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 136078943 | HCID 136078943 | 43.5% |
Reaction Steps
70 mg of 4-(6-hydroxyquinolin-2-yl)-3-methoxybenzoic acid (Compound 48) was suspended in 10 ml DCM and 0.25 ml BBr3 was added. The mixture was stirred at room temperature for 2 days. 20 ml water was added to quench the reaction. DCM was removed by evaporation and the precipitate was filtered and washed with water and dried to obtain 29 mg of 3-hydroxy-4-(6-hydroxyquinolin-2-yl)benzoic acid. 1H NMR (DMSO-d6 300 MHz TMS): δ 10.34 (s, 1H), 8.45 (d, 1H), 8.30 (d, 1H), 8.24 (d, 1H), 7.97 (d, 1H), 7.46 (m, 3H), 7.26 (d, 1H), MS (ESI): m/z=282.30 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09433618B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-23abbfb9931746fbb3e3490c2c0bbeb4 |
| Source note | uspto-grants-2016_09 |