HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113822Generated: October 25, 2026
Potassium Phosphate, Tribasic → 3-(4-Methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl ester
https://huagongshe.com/reaction/2113822
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-Bromo-4-(methylsulphonyl)benzene | HCID 77014 | — |
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Reactant | Methyl 3-hydroxy-5-(methoxymethoxy)benzoate | HCID 23136427 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(4-Methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl ester | HCID 59263314 | 71.1% |
Reaction Steps
After adding 33.4 g (142 mmol) of 4-methanesulfonyl-bromobenzene, 2.67 g (11.9 mmol) of palladium acetate, 5.31 g (17.8 mmol) of 2-(di-tert-butylphosphino)biphenyl and 50.3 g (237 mmol) of potassium phosphate to a solution of 25.0 g (119 mmol) of 5-hydroxy-3-methoxymethoxybenzoic acid methyl ester in toluene (375 ml), the reactor was sealed and the mixture was subsequently stirred at 130° C. for 6 hours. Acetic acid ethyl ester was added to the reaction mixture, which was then filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:acetic acid ethyl ester=2:1) to obtain 31.0 g of 3-(4-methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl ester (yield: 69%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432287B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-c299119bcbf2419e9ec0cb56e956bde2 |
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| Source note | uspto-grants-2008_10 |
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