Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965876Generated: October 30, 2026

Cyanoacetic acid → 2-cyano-3-[5-(9,9-dibutyl-7-dibutylamino-9H-fluoren-2-yl)-thiophen-2-yl]acrylic acid

https://huagongshe.com/reaction/1965876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetic acidHCID 9740—
ReactantHCID 86641779HCID 86641779—
CatalystPiperidineHCID 8082—
SolventAcetonitrileHCID 6342—
Product2-cyano-3-[5-(9,9-dibutyl-7-dibutylamino-9H-fluoren-2-yl)-thiophen-2-yl]acrylic acidHCID 66762275—

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 numberUS08419808B2
Source datasetuspto-grants-2013_04
ORD IDord-d7963c918ee14bd2875a138daec0cefd
Source noteuspto-grants-2013_04