Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Chloroform | HCID 6212 | — |
| Edukt | Methyl 10,12-pentacosadiynoate | HCID 145561 | — |
| Edukt | 10,12-Tricosadiynoic Acid | HCID 538457 | — |
| Katalysator | Sulfuric Acid | HCID 1118 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Methyl 10,12-tricosadiynoate | HCID 9968876 | — |
Reaktionsschritte
10,12-tricosadiynoic acid (10 gm, GFS Chemicals) was dissolved in a solution containing 10 ml methanol (HPLC grade) and 10 ml chloroform (HPLC grade). The solution was stirred at room temperature and 10 drops of neat sulfuric acid was added drop wise. The solution was warmed to 100° F. for 2 hour. The reaction mixture was purified using column chromatography. The product (MeTDA) was dried using a rotovap and the material stored in a chloroform solution. The solid form of MeTDA was very unstable to polymerization and therefore kept dissolved in organic solutions. Alcoholic solutions of MePDA and MeTDA: Solids MePDA or MeTDA were dissolved in reagent grade ethanol to a concentration of 150 mg/ml. An residual polymer was removed by filtration through Whatman No. 1 filter paper. The solutions was held at room temperature or slightly above (70-75° F.) to avoid crystallization or precipitation.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06607744B1 |
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| Quelldatensatz | uspto-grants-2003_08 |
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| ORD ID | ord-d9a79769612941789e4950af457834c4 |
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| Quellennotiz | uspto-grants-2003_08 |
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