Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Arachidonic Acid | HCID 444899 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Arachidonyl alcohol | HCID 10891603 | 99% |
Reaction Steps
To a suspension of LiAlH4 (0.499 g, 13.14 mmol) in dry THF (50 mL) was added arachidonic acid (1.00 g, 3.28 g) in dry THF (40 mL) at 0° C. (ice-bath) under argon and the reaction mixture was stirred for 1 h at 0° C. and then for 1 h at room temperature. After a slow addition of water (0.2 mL), the white gelatinious precipitate was dissolved by adding 10% aq NaOH (0.2 mL) and water (0.6 mL) and the mixture was allowed to stir for 1 h. The mixture was then dried over MgSO4, and filtered and the filtrate was concentrated under reduced pressure to furnish a crude, which was purified over silica-gel column chromatography using 20% ethyl acetate/hexane to give the product as a clear oil (0.945 g, 99%). 1H NMR (CDCl3): δ5.37 (m, 8H), 3.64 (t, 2H, J=6.4 Hz), 2.81 (m, 6H), 2.09 (m, 4H), 1.61 (m, 2H), 1.50-1.30 (m, 8H), 1.04 (t, 3H, J=6.8 Hz). m/z (APCI) 291.43 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563760B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-74970ca136ed4b73ad22ad6d9f2b5705 |
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| Source note | uspto-grants-2013_10 |
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