Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl arachidonate | HCID 6421258 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Arachidonyl alcohol | HCID 10891603 | 93% |
Reaction Steps
To a magnetically stirred solution of 0.5 ml (0.5 mmol) of LiAlH4 in Et2O, 100 mg (0.314 mmol) of arachidonic acid methyl ester in 2 mL of Et2O was added dropwise at 0° C. The reaction mixture was stirred for 1 h and then quenched by addition of 1 mL of EtOAC. 2 mL of saturated NH4Cl solution was added and the organic layer was separated, dried with MgSO4, filtered and evaporated. Chromatography on silica gel (eluents: CH2Cl2/petroleum ether up to 70% CH2Cl2), evaporation, followed by membrane filtration of a CH2Cl2 solution of the product gave 99.3 mg (0.292 mmol, 93% yield) of arachidonyl alcohol as a colorless oil: TLC (CHCl3) Rf 0.28; 1H NMR (200 MHZ, CDCl3) δ 5.37 (m, 8 H), 3.61 (t, 2 H, J=6 Hz), 2.79 (m, 6H), 2.08 (m, 4 H), 1.66–1.17 (m, 8H), 0.92 (t, 3H, J=7 Hz); Anal. C, H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07161016B1 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-5900ee2211d943f8a3d0a80e5cd0b58b |
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| Source note | uspto-grants-2007_01 |
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