Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Hexadecyloxy-3-triphenylmethoxypropan-2-one | HCID 21299162 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21299166 | HCID 21299166 | 82% |
Reaction Steps
A solution of n-butyllithium (47 ml, 113 mmol) in hexane was added to a suspension of methyltriphenylphosphonium bromide (40.0 g, 112 mmol) in 100 ml dry dioxane under N2 and the dark red solution was stirred at room temperature for 45 minutes. Compound 1 (35.1 g, 63.1 mmol) in 100 ml dry dioxane was added and the mixture was stirred for 2 hours. Water (10 ml) was added and the solution was partitioned between hexane and water. The aqueous layer was washed 2 times with hexane and the combined organic layers were dried over Na2SO4 and concentrated. The residue was crystallized from ethanol to afford 28.8 g (82%) of the title compound (2) as white needles, m.p. 34° ; NMR (CDCl3, (CH3)4Si); δ0.90 (t, 3H, J=6 Hz, --CH3), 1.25 (s, 26H, --CH2 --), 1.62 (m, 2H, --OCH2CH2R), 3.35 (t, 2H, J=7 Hz, --OCH2R), 3.62 (s, 2H, CH2OTr), 3.96 (s, 2 H, --CH2OR), 5.20 (d, 1 H, J=2 Hz, olefin), 5.40 (d, 1H, J=2 Hz, olefin), 7.2-7.5 (m, 15H, C(C6H5)85)3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04761404 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-1faf53b07d50474996f79a0d3787c674 |
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| Source note | uspto-grants-1988_08 |
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