Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phenoxyacetyl chloride | HCID 69703 | — |
| Reactant | HCID 86736556 | HCID 86736556 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 53987691 | HCID 53987691 | — |
Reaction Steps
13.5 g of the ketoaldehyde of formula XII obtained in Example 20 are dissolved in 100 ml of pyridine. 10 g of phenoxyacetic acid chloride are added dropwise to the solution at 0° C. The mixture is stirred for 1 hour at 0° C. and then poured into water and extracted with diethyl ether. The ether extract is washed with 5% strength aqueous sulfuric acid and then with water. The 5-[2,6,6-trimethyl-3-oxo-4(S)-(phenoxyacetoxy)-cyclohex-1-en-1-yl]-3-methyl-penta-2-en-4-yn-1-al (XIV) isolated from the extract is further reacted as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04156090 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-52bbec93df464e469252dc3f034b9100 |
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| Source note | uspto-grants-1979_05 |
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