Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Methyl (2E)-3-cyclohexylprop-2-enoate | HCID 5355239 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10396924 | HCID 10396924 | 82.2% |
Reaction Steps
29.25 g (0.174 mol) of (2E)-3-cyclohexylpropenoic acid methyl ester was dissolved in 200 ml of ether (dried over dry nap). Thereto was added 412 ml (0.383 mol) of diisobutylaluminum hydride (n-hexane solution, 0.93N) in an argon stream at -60° C. over a 15-minute period. The mixture was stirred at the same temperature for 30 minutes. n-Hexane and diethyl ether were added. The resulting mixture was washed with a saturated aqueous ammonium chloride solution, hydrochloric acid (0.2N) and a saturated aqueous sodium chloride solution, dried over magnesium sulfate, and concentrated. The concentrate was purified by silica gel column chromatography (n-hexane/ethyl acetate=19/1 to 9/1) and distillation (57.0°-58.5° C./0.40-0.42 mmHg) to obtain 20.1 g (0.143 mol) of (2E)-3-cyclohexyl-2-propen-1-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05545666 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-45fbe1b53df04e7ca9b0b3bd08a7f624 |
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| Source note | uspto-grants-1996_08 |
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