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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217598Generated: November 2, 2026

Methacryloyl chloride → HCID 22181556, compound

https://huagongshe.com/reaction/2217598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacryloyl chlorideHCID 13528—
ReactantSodium BicarbonateHCID 516892—
Reactant4'-Amino-3'-fluoro-biphenyl-2-sulfonic acid tert-butylamideHCID 10853284—
SolventEthyl AcetateHCID 8857—
ProductHCID 22181556HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407974B2
Source datasetuspto-grants-2008_08
ORD IDord-eb260c7244a54f89aa16571b4a8672bf
Source noteuspto-grants-2008_08