HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 5-Bromo-2-fluoro-4-hydroxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-Fluoro-4-methoxybenzaldehyde | HCID 2734873 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-2-fluoro-4-hydroxybenzaldehyde | HCID 59342578 | 80.6% |
Reaction Steps
To the solution of 2-fluoro-4-methoxybenzaldehyde (3 g, 19.5 mmol, 1 eq., Aldrich, Milwaukee, Wis., USA) in DCM (80 mL) was added dropwise BBr3 (14.5 g, 58.7 mmol, 3 eq.) at 0° C. The mixture was stirred for 15 min, then warmed to room temperature and continued to stir for additional 3 h. The reaction was quenched by careful addition of water (50 mL), the organic layer was separated, and remaining the aqueous layer was extracted with DCM (2×50 mL). The combined organic layers were concentrated in vacuo and purified by silica gel chromatography (DCM:MeOH=25:1 to 10:1) to afford 2.2 g (80.6%) of 2-fluoro-4-hydroxybenzaldehyde (24).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822467B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-ff4775306e1648ceb8f3dbdcd30d6e7d |
| Source note | uspto-grants-2014_09 |