HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl iodide → (7-bromo-9H-fluoren-2-yl)-dibutyl amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | 2-Amino-7-bromofluorene | HCID 23126 | — |
| Product | (7-bromo-9H-fluoren-2-yl)-dibutyl amine | HCID 59325934 | — |
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 | US08203068B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-bfb92b2ec61f4d0987952e2aab2837d9 |
| Source note | uspto-grants-2012_06 |