Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Lauric Acid | HCID 3893 | — |
| Reactant | Bis(eta-cyclopentadienyl) iron | HCID 7611 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178443271 | HCID 178443271 | 87% |
Reaction Steps
8.01 g of lauric acid was added to 100 ml of 85% phosphoric acid and 100 g of polyphosphoric acid, and heated at 180° C. for three hours while the pressure was reduced (1 mmHg) with the use of vacuum pump. After the mixture was cooled, 1.86 g of ferrocene and 20 ml of methylene chloride were added, and the resulting mixture was heat-refluxed at 50° C. for 9 hours. Then, the mixture was poured into water, and made to be basic with potassium hydroxide, and subjected to extraction with methylene chloride, and dried. The unreacted ferrocene was removed by a column chromatography, to obtain 3.20 g of undecanylferrocenyl ketone represented by the formula (A) in a yield of 87.0%. The proton nuclear magnetic resonance (1H--NMR) spectrum of the product is shown in FIG. 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05110964 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-987bc769bfb94a778b5c30bf709b18a5 |
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| Source note | uspto-grants-1992_05 |
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