HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyltrimethylsilane → [(5-Hexylthiophen-2-yl)ethynyl](trimethyl)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyltrimethylsilane | HCID 137936 | — |
| Reactant | 2-Bromo-5-hexylthiophene | HCID 10562418 | — |
| Product | [(5-Hexylthiophen-2-yl)ethynyl](trimethyl)silane | HCID 68743804 | 101.1% |
Reaction Steps
According to the method described in S117a, 2-bromo-5-hexylthiophene (1 g, 4 mmol) was reacted with trimethylsilylethane (0.43 g, 4.4 mmol) to give the title compound as a yellow oil (1.07 g, 100%). 1H NMR (400 MHz, CDCl3) δ 7.05 (d, 1H, J=3.6 Hz), 6.61 (d, 1H, J=3.6 Hz), 2.77 (t, 2H, J=7.2 Hz) 1.65-1.56 (m, 2H), 1.36-1.30 (m, 6H), 0.89 (t, 3H, J=6.4 Hz), 0.24 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410150B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-e0e5bb213d31495bac77b4fd8a4661e1 |
| Source note | uspto-grants-2013_04 |