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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70004Generated: October 28, 2026

N-Iodosuccinimide → HCID 89645354, compound

https://huagongshe.com/reaction/70004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactantalpha-(Cyclopropylsulfonyl)phenylacetic acidHCID 89645031—
ProductHCID 89645354HCID 8964535432%

Reaction Steps

However, the use of these reagents as source of iodine for reactions of iodo-de-carboxylation are limited. Reaction of N-halosuccinimides with aryl acrylic and aryl propiolic acids gives 1-halo-2-aryl-1-alkenes and 1-halo-2-aryl-1-alkynes (J. Org. Chem. 2002, v. 67, 7861; J. Org. Chem. 1999, v. 64, 6896; J. Org. Chem. 1997, v. 62, 199; Tetrahedron 2000, v. 56, 1369). All the reactions occur in the presence of catalyst. Reaction of α-(cyclopropylsulfonyl)phenylacetic acid with NIS gives α-iodobenzyl cyclopropyl sulfone only with 32% yield (J. Org. Chem. 1974, v. 39, 2516).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822516B2
Source datasetuspto-grants-2014_09
ORD IDord-ebea337bce0c441ab30dcbb724572369
Source noteuspto-grants-2014_09