Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965878Generated: October 27, 2026

Butyl iodide → 9,9-dibutyl-2-iodo-9H-fluorene

https://huagongshe.com/reaction/1965878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
Reactant2-Iodo-9H-fluoreneHCID 224094—
Product9,9-dibutyl-2-iodo-9H-fluoreneHCID 23072853—

Reaction Steps

As shown in Scheme 3, 7-bromo-9H-fluoren-2-ylamine is reacted with 1-iodobutane to form 7-bromo-9,9-dibutyl-9H-fluoren-2-ylamine (31); and 2-Iodo-9H-fluorene is reacted with 1-iodobutane to form 9,9-dibutyl-2-iodo-9H-fluorene (32). Then, 7-bromo-9,9-dibutyl-9H-fluoren-2-ylamine (31) is reacted with 9,9-dibutyl-2-iodo-9H-fluorene (32) by Ullman coupling reaction to obtain (7-bromo-9,9-dibutyl-9H-fluoren-2-yl)-bis-(9,9-dibutyl-9H-fluoren-2-yl)amine (33). Next, (7-bromo-9,9-dibutyl-9H-fluoren-2-yl)-bis-(9,9-dibutyl-9H-fluoren-2-yl)amine (33) is reacted with 5-formyl-2-thiopheneboronic acid by Suzuki coupling reaction to obtain 5-{7-[bis-(9,9-dibutyl-9H-fluoren-2-yl)amino]-9,9-dibutyl-9H-fluoren-2-yl}-thiophene-2-carbaldehyde (34a). Finally, in acetonitrile, 5-{7-[bis-(9,9-dibutyl-9H-fluoren-2-yl)amino]-9,9-dibutyl-9H-fluoren-2-yl}-thiophene-2-carbaldehyde (34a) is reacted with cyanoacetic acid by using piperidine as a catalyst, to obtain 3-(5-{7-[bis-(9,9-dibutyl-9H-fluoren-2-yl)amino]-9,9-dibutyl-9H-fluoren-2-yl}-thiophen-2-yl)-2-cyano-acrylic acid (35a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08419808B2
Source datasetuspto-grants-2013_04
ORD IDord-11ccc3433f2e4a08b10342a07a485561
Source noteuspto-grants-2013_04