Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221163Generated: October 25, 2026

5-Formyl-2-thiopheneboronic acid → HCID 86641779, compound

https://huagongshe.com/reaction/221163

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Formyl-2-thiopheneboronic acidHCID 2773430—
Reactant(7-bromo-9,9-dibutyl-9H-fluoren-2-yl)-dibutylamineHCID 58239559—
ProductHCID 86641779HCID 86641779—

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-ed18a9fb90b748e6b4ffd28e78b67a13
Source noteuspto-grants-2012_06