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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452735Generated: October 27, 2026

2-Iodoaniline → HCID 25159658, compound

https://huagongshe.com/reaction/1452735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodoanilineHCID 11995—
Reactant1-Ethenyl-4-ethynylbenzeneHCID 10942441—
ProductHCID 25159658HCID 2515965872%

Reaction Steps

The general procedure was used to convert 1-Ethynyl-4-vinyl-benzene and 2-iodoaniline to the title product. Purification by flash chromatography gave the analytically pure product as a white solid, 72% yield. 1H NMR (300 MHz, CDCl3) δ 8.31 (s, br, 1H), 7.64-7.61 (d, J=8.29, 3H), 7.49-7.46 (d, J=8.29, 2H), 7.40-7.38 (d, J=8.10, 1H), 7.22-7.16 (dt, J=6.97, 1H), 7.14-7.09 (dt, J=7.91, 1H), 6.84 (s, 1H), 6.78-6.69 (dd, J=10.73, 1H), 5.82-5.76 (dd, J=17.70, 1H), 5.30-5.26 (dd, J=10.73, 1H). Anal. Calcd. for C16H13N: C, 87.64; H, 5.98; N, 6.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473786B1
Source datasetuspto-grants-2009_01
ORD IDord-92bad07d88994efd953bbe8cf9598db9
Source noteuspto-grants-2009_01