Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Hexylthiophene | HCID 87793 | 75% |
Reaction Steps
To a solution of thiophene (15 g, 0.178 mole) in 200 mL of dry THF at −78° C., n-BuLi (103 mL, 0.165 mol, 1.6M hexane) was added. The reaction mixture was warmed to RT and stirred for 1 h. After the mixture was cooled to −78° C., 23.15 mL (0.165 mole) of 1-bromohexane was added. The solution was warmed from −78° C. to RT and was stirred overnight. At the end of the reaction, the mixture was poured into ice water, the aqueous layer was extracted with ether, and the organic layer was dried over anhydrous MgSO4. The solvent was removed by rotary evaporation. The residue was redistilled under vacuum to get a colorless liquid (yield=75%). 1H-NMR (300 MHz, CDCl3) δ 7.12 (dd, 1H), 6.92-6.97 (m, 1H), 6.8 (dd, 1H). 2.8 (t, 2H), 1.6-1.9 (q, 2H), 1.30-1.49 (m, 6H), 0.82 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618298B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-fd6aa4a1862e45209729fedb8fd76397 |
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| Source note | uspto-grants-2013_12 |
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