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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221162Generated: November 1, 2026

Butyl iodide → (7-bromo-9,9-dibutyl-9H-fluoren-2-yl)-dibutylamine

https://huagongshe.com/reaction/221162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
Reactant2-Amino-7-bromofluoreneHCID 23126—
Product(7-bromo-9,9-dibutyl-9H-fluoren-2-yl)-dibutylamineHCID 58239559—

Reaction Steps

As shown in Scheme 2, 7-bromo-9H-fluoren-2-ylamine is reacted with 1-iodobutane to form (7-bromo-9,9-dibutyl-9H-fluoren-2-yl)-dibutylamine (21). Then, (7-bromo-9,9-dibutyl-9H-fluoren-2-yl)-dibutylamine (21) is reacted with 5-formyl-2-thiopheneboronic acid by Suzuki coupling reaction to obtain 5-(9,9-Dibutyl-7-dibutylamino-9H-fluoren-2-yl)-thiophene-2-carbaldehyde (22a). Finally, in acetonitrile, 5-(9,9-Dibutyl-7-dibutylamino-9H-fluoren-2-yl)-thiophene-2-carbaldehyde (22a) is reacted with cyanoacetic acid by using piperidine as a catalyst, to obtain 2-Cyano-3-[5-(9,9-dibutyl-7-dibutylamino-9H-fluoren-2-yl)-thiophen-2-yl]-acrylic acid (23a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08203068B2
Source datasetuspto-grants-2012_06
ORD IDord-5fce3db293b743f294c6f6485994e3e3
Source noteuspto-grants-2012_06