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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710286Generated: October 26, 2026

5-Iodo-1H-indole → 5-(Oct-1-ynyl)-1H-indole

https://huagongshe.com/reaction/710286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Iodo-1H-indoleHCID 2782313—
Reactant5-Iodo-2-tritylisoindolineHCID 66726248—
Product5-(Oct-1-ynyl)-1H-indoleHCID 6672675136%

Reaction Steps

When 5-iodo-1H-indole was substituted for 5-iodo-2-tritylisoindoline in Example 2, Step D, the identical process afforded the title compound in 36% yield. 1H-NMR (CDCl3) 0.9 (tr, 3H, J=6.9 Hz); 1.31 (m, 6H); 1.46 (m, 2H); 1.6 (m, 2H); 2.41 (tr, 2H, J=7.1 Hz); 6.49 (m, 1H); 7.14-7.31 (m, 3H); 7.71 (s, 1H); 8.13 (broad s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181182B2
Source datasetuspto-grants-2015_11
ORD IDord-2dff5ecba5e14ad7b9d30b9545ad7987
Source noteuspto-grants-2015_11