Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 70631652 | HCID 70631652 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70631647 | HCID 70631647 | — |
Reaction Steps
A solution of 0.75 g. of 7-(3-hydroxy-1-octenyl)-1,4-dioxaspiro[4.4]non-6-ylheptanoic acid in 40 ml. of acetone was cooled to 0° C. and treated with 2.0 ml. of Jones Reagent. After stirring for 10 minutes, at 0° C., the reaction mixture was treated with 5 ml. of methanol, dilute sodium bicarbonate until basic and water. Following acidification with acetic acid, the mixture was extracted with ether and the extract washed with water, dried and evaporated. Silica chromatography of the resulting residue with 30% ethyl acetate-hexane gave 0.355 g. of the title product, λmaxfilm 3.1 (shoulder), 5.8, 6.1, 6.75, 8.6, 9.6, 10.1, 10.5 μ. NMR: δ 6.78 (dd, 1, J=8.3, 15.8, 13-H), 6.18 (d, 1, J-15.8, 14-H), 3.92 (S, 4, ketal) ppm. UV: λmaxEtOH 230 mμ (ε 10,000). Mass spectrum N+ at m/c 380.2523 (theory 380.2562).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04011338 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-dbfbcc8f95ec428fa84cd35d9ec8d1ce |
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| Source note | uspto-grants-1977_03 |
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