HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanoacetic acid → 2-cyano-3-[5-(7-dibutylamino-9H-fluoren-2-yl)-thiophen-2-yl]-acrylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | 5-(7-dibutylamino-9H-fluoren-2-yl)-thiophene-2-carbaldehyde | HCID 86641778 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-cyano-3-[5-(7-dibutylamino-9H-fluoren-2-yl)-thiophen-2-yl]-acrylic acid | HCID 66762166 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08419808B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-63a4874a61c4458b9dd28b24cea18349 |
| Source note | uspto-grants-2013_04 |