Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl propiolate | HCID 13536 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 14722268 | HCID 14722268 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 14722307 | HCID 14722307 | 31.6% |
Reaction Steps
3 g of 4-(2,4-difluorophenoxy)-3-methylsulfonylaminophenol was dissolved in 15 ml of N,N-dimethylformamide. 420 mg of sodium hydride (purity: 60%) was added. The mixture was stirred for 20 minutes at 20-25° C. Then, 0.88 g of methyl propiolate was added dropwise in about 5 minutes so that the reaction temperature was maintained below 40° C. The mixture was stirred for 30 minutes at 30°-40° C. After the completion of the reaction, 50 ml of water and 50 ml of ethyl acetate were added thereto. The resulting mixture was adjusted to pH 4 with 4N hydrochloric acid. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried with anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and the residue was purified by a column chromatography (eluant: a 20:1 mixture of toluene and ethyl acetate) to obtain 1.2 g (yield: 31.6%) of methyl trans-3-[4-(2,4-difluorophenoxy)-3-methylsulfonylaminophenoxy]acrylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04954518 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-78d17bccbe5f4f46a3052a45ab325c11 |
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| Source note | uspto-grants-1990_09 |
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