Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 13058-52-1 | HCID 11748436 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 11565215 | HCID 11565215 | 92.1% |
Reaction Steps
To a suspension of lithium aluminum hydride (1.5 g, 38.7 mmol) in anhydrous ether (50 mL) cooled to 0° C. under nitrogen was slowly added a solution of (9Z,11E)-methyl octadeca-9,11-dienoate (11.6 g, 38.7 mmol) in anhydrous diethyl ether (50 mL+25 mL rinse) via cannula transfer. The solution was stirred for 2 hours at 0° C. then quenched slowly with 1M NaOH (3.5 mL). The solution was dried on magnesium sulfate, filtered and concentrated in vacuo to dryness to afford the product as a colorless oil (9.5 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865675B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-6bf3acd359944be5a6cb5e06873c4c6d |
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| Source note | uspto-grants-2014_10 |
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