Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Periodate | HCID 167232 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Reactant | HCID 70372852 | HCID 70372852 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86737257 | HCID 86737257 | 65% |
Reaction Steps
A mixture of 5-ethylenedioxy-1-hexene (6.0 g.), osmium tetroxide (0.5 g.) , ether (150 ml.) and water (150 ml.) is treated portionwise with sodium metaperiodate (19.3 g.) so that the reaction temperature does not exceed 30°. After the addition of the periodate, a voluminous white solid precipitates out. The mixture is stirred 2.5 hrs. at room temperature, then filtered, and the solid portion is washed with more aqueous ether. The aqueous portion of the filtrate is separated and extracted with three portions of methylene chloride. The combined organic phases are dried with magnesium sulfate, filtered, and evaporated in vacuo. Distillation of the residue yields 4-ethylenedioxy-pentanal (65% yield) b.p. 56°-58°/10.5 mm nmr (CDCl3)δ: 1.27 (s, CH3), 2.04-2.80 (m, --CH2 --CH2 --); 3.9 (s, --OCH2 --CH2 --O), 9.73 (t, O=C--H). IR (film) μ: 3.66; 3.79.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04226866 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-050cd6f77ae94d519f392449ebbb8b77 |
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| Source note | uspto-grants-1980_10 |
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