HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-3-Dodecylthiophene → HCID 59428851, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-3-Dodecylthiophene | HCID 10426816 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Product | HCID 59428851 | HCID 59428851 | 34% |
Reaction Steps
A reaction between 2-bromo-3-dodecylthiophene (Compound-1, 81.0 mmol) and excess copper cyanide (CuCN) produced 2-cyano-3-dodecylthiophene (Compound-2, 34% yield), which was heated and reacted with excess (approximately 2.5 equivalents) dithiophosphoric acid O,O′-diethylether in tetrahydrofuran (THF) solution for about 12 hours. The obtained 2-thioamino-3-dodecylthiophene (Compound-3, 45% yield) and 1.2 equivalents of bromooctanone were reacted to obtain 2-thiazole(3′-dodecyl)-3-dodecylthiophene (Compound-4, 32% yield), which was in turn reacted with N-bromosuccinimide (NBS) to obtain the thiophene-thioazol derivative (Compound-5, 82% yield). An NMR analysis result of the resultant product was as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07777221B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-9003604b5c7549a4bcfb551a9c37a668 |
| Source note | uspto-grants-2010_08 |