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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824880Generated: October 25, 2026

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

https://huagongshe.com/reaction/1824880

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorobenzenesulfonamideHCID 519377—
Reactant3-[4-(Z)-(1,2-diphenylbut-1-enyl)phenyl]-acrylic acidHCID 3036152—
Product3-chloro-N-{3-[4-(1,2-diphenyl-but-1-enyl)-phenyl]-acryloyl}-benzenesulfonamideHCID 69315997—

Reaction Steps

Prepared by coupling 1a and 3-chlorobenzenesulfonamide in accordance with Procedure 1, Method B described hereinabove. Yield (25%); 1H NMR (d6-DMSO) δ 12.36 (s, 1H), 7.88–7.76 (m, 3H), 7.63 (t, J=8.1 Hz, 1H), 7.42–7.07 (m, 13H), 6.84 (d, J=8.0 Hz, 2H), 6.40 (d, J=15.7 Hz, 1H), 2.36 (q, J=7.3 Hz, 2H), 0.82 (t, J=7.3 Hz, 3H); APcI m/z: 527 (M−H−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045540B2
Source datasetuspto-grants-2006_05
ORD IDord-070134cd367349db9cc6d792cf5caf58
Source noteuspto-grants-2006_05