Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 86689404 | HCID 86689404 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86689405 | HCID 86689405 | 82.4% |
Reaction Steps
n-BuLi (2.5 M in hexanes, 261 cm3, 652 mmol) is added dropwise over 60 minutes to a solution of 7-(2,2-dibromo-vinyl)-pentadecane (4.1) (117 g, 296 mmol) in anhydrous tetrahydrofuran (1350 cm3) at −78° C. The mixture is stirred for 45 minutes at −78° C. and water (1.3 L) is carefully added. The reaction mixture exotherms to −10° C. and is allowed to warm to 23° C. whilst stirring over 18 hours. The organic phase is separated, washed with brine (1500 cm3), dried over sodium sulfate, filtered and concentrated in vacuo. The crude oil is passed through a plug of silica eluting with petroleum ether (40-60° C.). The pale yellow oil is further purified by distillation under vacuum (96° C. at 0.85 mmHg) to give the title product as a colourless oil (57.7 g, Yield: 82%). NMR (1H, 300 MHz, CDCl3): δ 2.30 (m, 1H); 2.03 (d, J=2.4 Hz, 1H); 1.44 (m, 8H); 1.27 (m, 16H); 0.88 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09287504B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-dc2378b626f4465d8fc8eb8f7147187b |
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| Source note | uspto-grants-2016_03 |
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