HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161512Generated: October 28, 2026
Hydrochloric Acid → 3-Fluoro-6-methoxy-2-vinylphenol
https://huagongshe.com/reaction/1161512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 6-Fluoro-2-hydroxy-3-methoxybenzaldehyde | HCID 22482818 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Fluoro-6-methoxy-2-vinylphenol | HCID 67097333 | — |
Reaction Steps
To a suspension of 50 g of methyltriphenylphosphonium bromide in 300 ml of toluene there was added dropwise 45 ml of n-butyllithium (2.55 M, hexane solution) at 0° C. under a nitrogen atmosphere. The mixture was stirred at room temperature for 2 hours and allowed to stand. Next, 150 ml of the supernatant was added to a solution of 5 g of 6-fluoro-2-hydroxy-3-methoxybenzaldehyde [CAS No. 457628-15-8] in 90 ml of toluene. The mixture was stirred at room temperature for 1 hour, 1N hydrochloric acid was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give 3-fluoro-6-methoxy-2-vinylphenol (4.33 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07816522B2 |
|---|
| Source dataset | uspto-grants-2010_10 |
|---|
| ORD ID | ord-770117bac6f144d2b9006bfd195dd09d |
|---|
| Source note | uspto-grants-2010_10 |
|---|