HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Formyl-2-thiopheneboronic acid → HCID 86641779, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Formyl-2-thiopheneboronic acid | HCID 2773430 | — |
| Reactant | (7-bromo-9,9-dibutyl-9H-fluoren-2-yl)-dibutylamine | HCID 58239559 | — |
| Product | HCID 86641779 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08203068B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-ed18a9fb90b748e6b4ffd28e78b67a13 |
| Source note | uspto-grants-2012_06 |