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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824874Generated: October 25, 2026

4-Nitrobenzenesulfonamide → N-{3-[4-(1,2-diphenyl-but-1-enyl)-phenyl]-acryloyl}-4-nitro-benzenesulfonamide

https://huagongshe.com/reaction/1824874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzenesulfonamideHCID 22784—
Reactant3-[4-(Z)-(1,2-diphenylbut-1-enyl)phenyl]-acrylic acidHCID 3036152—
ProductN-{3-[4-(1,2-diphenyl-but-1-enyl)-phenyl]-acryloyl}-4-nitro-benzenesulfonamideHCID 69780499—

Reaction Steps

Prepared by coupling 1a and 4-nitrobenzenesulfonamide in accordance with Procedure 1, Method A described hereinabove. Yield (32%); 1H NMR (d6-DMSO) δ 8.33 (d, J=8.8 Hz, 2H), 8.08 (d, J=8.8 Hz, 2H), 7.38–7.07 (m, 13H), 6.82 (d, J=8.0 Hz, 2H), 6.35 (d, J=15.7 Hz, 1H), 2.35 (q, J=7.3 Hz, 2H), 0.81 (t, J=7.3 Hz, 3H); APcI m/z: 538 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045540B2
Source datasetuspto-grants-2006_05
ORD IDord-4ccfb4a47e9641bd98a3b6ed72586af3
Source noteuspto-grants-2006_05