Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydroxyphenylacetic acid | HCID 127 | — |
| Edukt | Myristyl bromide | HCID 8208 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Katalysator | Trioctadecyl methylamine chloride | HCID 131715051 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | p-Tetradecyloxyphenylacetic acid | HCID 10472964 | 38,4% |
Reaktionsschritte
A mixture of about 75 g of 4-hydroxyphenylacetic acid, about 273.38 g of 1-tetradecylbromide, about 46.33 g of sodium hydroxide, about 5.0 g of trioctadecyl methylamine chloride and about 500 ml of water was refluxed for about 24 hours with stirring, cooled to room temperature, the aqueous layer decanted and the solid washed with water. The solid was refluxed for about 2 hours with stirring in about 500 ml of ethanol containing about 40 g of sodium hydroxide and about 40 ml of water. The solvents were removed and the residue heated at about 0.1 mm and about 200°-210° C. in a Kugelrohr. The residue was stirred with dilute hydrochloric acid and ethyl acetate on a steam bath until solution was complete. The warm solution was washed with brine, then the solvent was removed and the residue recrystallized sequentially from methanol and hexane, giving about 66 g of the desired title compound as a white solid, mp 86°-87° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04640913 |
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| Quelldatensatz | uspto-grants-1987_02 |
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| ORD ID | ord-da2ad265cd6e4817bd16622f17529c16 |
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| Quellennotiz | uspto-grants-1987_02 |
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