HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-Fluoro-2-hydroxy-3-methoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | 6-Fluoro-2,3-dimethoxybenzaldehyde | HCID 10726148 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Fluoro-2-hydroxy-3-methoxybenzaldehyde | HCID 22482818 | 95.1% |
Reaction Steps
1M boron trichloride in dichloromethane (25 ml; 25 mmol) was added to a solution of 6-fluoro-2,3-dimethoxy-benzaldehyde [Cantrell, Amanda S.; Engelhardt, Per; Hoegberg, Marita; Jaskunas, S. Richard; Johansson, Nils Gunnar; et al.; J. Med. Chem.; 39; 21; 1996; 4261-4274] (4.26 g; 23 mmol) in dichloromethane (30 ml) keeping the reaction temperature at −70° C. The reaction mixture stirred at room temperature overnight and hydrolyzed with water. The organic phase was separated, washed with water and evaporated in vacuo. The residue was chromatographed (silica gel, EA:Hex, 5:1) to give 3.72 g (94%) of 6-fluoro-2-hydroxy-3-methoxy-benzaldehyde as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915295B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-7b7de126cb8a426db9700fa85a299413 |
| Source note | uspto-grants-2011_03 |