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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824872Generated: October 25, 2026

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

https://huagongshe.com/reaction/1824872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrobenzenesulfonamideHCID 138510—
Reactant3-[4-(Z)-(1,2-diphenylbut-1-enyl)phenyl]-acrylic acidHCID 3036152—
ProductN-{3-[4-(1,2-diphenyl-but-1-enyl)-phenyl]-acryloyl}-2-nitro-benzenesulfonamideHCID 69781207—

Reaction Steps

Prepared by coupling 1a and 2-nitrobenzenesulfonamide in accordance with Procedure 1, Method B described hereinabove. Yield (22%); 1H NMR (d6-DMSO) δ 8.18 (d, J=5.2 Hz, 1H), 7.99 (d, J=5.9 Hz, 1H), 7.94–7.84 (m, 2H), 7.44–7.08 (m, 13H), 6.86 (d, J=8.1 Hz, 2H), 6.50 (d, J=15.7 Hz, 1H), 2.36 (q, J=7.4 Hz, 2H), 0.82 (t, J=7.4 Hz, 3H); APcI m/z: 539 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045540B2
Source datasetuspto-grants-2006_05
ORD IDord-9abc4a094bfe44e1b5660abb4bab97eb
Source noteuspto-grants-2006_05