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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253467Generated: October 26, 2026

3-[4-(Z)-(1,2-diphenylbut-1-enyl)phenyl]-acrylic acid → N-{3-[4-(1,2-diphenyl-but-1-enyl)-phenyl]-acryloyl}-3-methoxy-benzenesulfonamide

https://huagongshe.com/reaction/2253467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[4-(Z)-(1,2-diphenylbut-1-enyl)phenyl]-acrylic acidHCID 3036152—
Reactant3-Methoxybenzene-1-sulfonamideHCID 14763060—
ProductN-{3-[4-(1,2-diphenyl-but-1-enyl)-phenyl]-acryloyl}-3-methoxy-benzenesulfonamideHCID 69780580—

Reaction Steps

Prepared by coupling 1a and 3-methoxybenzenesulfonamide (Synlett, 1997, 375) in accordance with Procedure 1, Method B describe hereinabove. Yield (27%); 1H NMR (d6-DMSO) δ 12.18 (br s, 1H), 7.53-7.07 (m, 17H), 6.84 (d, J=8.0 Hz, 2H), 6.40 (d, J=15.7 Hz, 1H), 3.78 (s, 3H), 2.35 (q, J=7.4 Hz, 2H), 0.82 (t, J=7.4 Hz, 3H); APcI m/z: 522 (M−H−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323587B2
Source datasetuspto-grants-2008_01
ORD IDord-21f2f4dca4e548738f207d6cd907e106
Source noteuspto-grants-2008_01