HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217489Generated: November 2, 2026
Methacryloyl chloride → HCID 22181556, compound
https://huagongshe.com/reaction/2217489
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4'-Amino-3'-fluoro-biphenyl-2-sulfonic acid tert-butylamide | HCID 10853284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22181556 | HCID 22181556 | — |
Reaction Steps
To 4′-Amino-3′-fluoro-biphenyl-2-sulfonic acid tert-butylamide (5.000 g, 15.51 mmoles) at room temperature in ethyl acetate (50 ml) was added saturated sodium bicarbonate, aqueous, 50 ml and then 2-methyl-acryloyl chloride (1.25 equiv.). Stirred for 2 hours then added a further 1 ml of the acid chloride. After 2 hours an aliquot showed product by NMR. Product seems to co-run with starting material. Extracted into ethyl acetate, washed with brine, dried MgSO4, and then concentrated in vacuo. Collected some crystalline product from ethyl acetate hexane, 0.48 g. Columned mother liquor to afford product. Combined with previously crystallized fraction to afford N-(2′-tert-Butylsulfamoyl-3-fluoro-biphenyl-4-yl)-2-methyl-acrylamide (4.520 g). APCI (AP+): 391 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07407972B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-279a7bd2e60a49d3984d680ce45f4964 |
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| Source note | uspto-grants-2008_08 |
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