Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Phosphoric Acid | HCID 1004 | — |
| Edukt | 1-Benzylnaphthalene | HCID 38074 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-Benzyl-2-chloromethylnaphthalene | HCID 22119573 | 32% |
Reaktionsschritte
1-Benzylnaphthalene (3.0 g; 13.7 mMol), as prepared above, formaldehyde (1.0 g; 35.7 mMol), glacial acetic acid (4.3 g; 71.7 mMol), concentrated hydrochloric acid (6.5 mL) and 85% phosphoric acid (4.3 mL) were combined and heated in an oil bath maintained at 90° C. for 4.5 hr. The reaction mixture was cooled, a small amount of water was added, and extraction was carried out with diethyl ether. The combined organic extractions were washed with sodium carbonate (10% aqueous), and brine; then dried over magnesium sulfate. The solvent was removed under reduced pressure, and the residue subjected to medium pressure chromatography on silica gel eluting with hexane. The product (1.18 g; 32% yield) was isolated as a colorless oil which subsequently crystallized.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06160175 |
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| Quelldatensatz | uspto-grants-2000_12 |
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| ORD ID | ord-703b44c124f74a87a1d4ca06178ead62 |
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| Quellennotiz | uspto-grants-2000_12 |
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