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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221160Generated: October 25, 2026

5-Formyl-2-thiopheneboronic acid → 5-(7-dibutylamino-9H-fluoren-2-yl)-thiophene-2-carbaldehyde

https://huagongshe.com/reaction/221160

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Formyl-2-thiopheneboronic acidHCID 2773430—
Reactant(7-bromo-9H-fluoren-2-yl)-dibutyl amineHCID 59325934—
Product5-(7-dibutylamino-9H-fluoren-2-yl)-thiophene-2-carbaldehydeHCID 86641778—

Reaction Steps

As shown in Scheme 1, 7-bromo-9H-fluoren-2-ylamine is reacted with 1-iodobutane to form (7-bromo-9H-fluoren-2-yl)-dibutyl amine (11). Then, (7-bromo-9H-fluoren-2-yl)-dibutyl amine (11) is reacted with 5-formyl-2-thiopheneboronic acid by Suzuki coupling reaction to obtain 5-(7-dibutylamino-9H-fluoren-2-yl)-thiophene-2-carbaldehyde (12a). Finally, in acetonitrile, 5-(7-dibutylamino-9H-fluoren-2-yl)-thiophene-2-carbaldehyde (12a) is reacted with cyanoacetic acid by using piperidine as a catalyst, to obtain 2-cyano-3-[5-(7-dibutylamino-9H-fluoren-2-yl)-thiophen-2-yl]-acrylic acid (13a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08203068B2
Source datasetuspto-grants-2012_06
ORD IDord-15942080ca424e1ab37ecf927f7831ae
Source noteuspto-grants-2012_06