Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxypropene | HCID 8300 | — |
| Reactant | 3-Nonen-5-ol, 4,8-dimethyl- | HCID 54316877 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 53705091 | HCID 53705091 | — |
Reaction Steps
10 g of 2,6-dimethyl-6-nonen-5-ol and 12 7 g of isopropenyl methyl ether are mixed and treated with 3 drops of concentrated hydrochloric acid. The mixture is subsequently held at reflux temperature for 15 hours, cooled, taken up in hexane and washed neutral with sodium hydrogen carbonate solution and water. After distillation of the solvent, there are obtained 14.1 g of crude 5-[1'-methoxy-1'-methyl-ethoxy]-2,6-dimethyl-6-nonene which are rectified in a water-jet pump vacuum (boiling point 109° C./12 Torr, nD20 =1.4379). The mixed acetal decomposes when subjected to gas chromatography and must therefore be tested for purity by thin-layer chromatography (elution agent: hexane/pentane/chloroform/ethyl acetate in the ratio 25:25:50:5); Rf =0.60.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04948781 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-be8a1c3df996470dbca9ac9f7749b311 |
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| Source note | uspto-grants-1990_08 |
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