HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354995Generated: October 31, 2026
Ethyl Acetate → 3-(3-Fluoro-4-methanesulfonyl-phenoxy)-5-methoxymethoxybenzoic acid methyl ester
https://huagongshe.com/reaction/2354995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Reactant | 3-(4-Bromo-3-fluoro-phenoxy)-5-methoxymethoxybenzoic acid methyl ester | HCID 68708471 | — |
| Reactant | brine NH4OH | HCID 131727087 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-(3-Fluoro-4-methanesulfonyl-phenoxy)-5-methoxymethoxybenzoic acid methyl ester | HCID 68704714 | 48% |
Reaction Steps
After adding 757 mg (7.41 mmol) of sodium methanesulfinate and 1.41 g (7.41 mmol) of copper iodide to a solution of 357 mg (0.93 mmol) of the obtained ester compound in dimethylsulfoxide (6.0 ml), the reaction mixture was stirred at 120° C. for 6 hours. Sodium chloride water-ammonia water (9:1) was added to the reaction mixture and extraction was performed with acetic acid ethyl ester, and then the organic layer was washed with brine, dried and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:acetic acid ethyl ester=2:1) to obtain 170 mg of 3-(3-fluoro-4-methanesulfonyl-phenoxy)-5-methoxymethoxybenzoic acid methyl ester (yield: 48%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07754743B2 |
|---|
| Source dataset | uspto-grants-2010_07 |
|---|
| ORD ID | ord-fb3c77bbe7944fc1b8fa9abe353f6c0d |
|---|
| Source note | uspto-grants-2010_07 |
|---|