Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenol | HCID 996 | — |
| Edukt | Diethyl disulfide | HCID 8077 | — |
| Katalysator | Zirconium chloride (ZrCl4), (T-4)- | HCID 9856075 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | 2-(Ethylthio)phenol | HCID 122407 | 44,1% |
Reaktionsschritte
A mixture of phenol (87.5 g, 0.93 moles), xylene (100 ml), and zirconium tetrachloride (6.0 g, 0.026 moles) was heated to reflux under a slow nitrogen stream. The xylene was distilled through a 10 inch Vigreux column. The distillation was continued over a 2 hour period until the reaction mixture reached 177° C. Approximately 10 g of phenol was distilled with the xylene. The reaction mass was cooled to 150° C., and ethyl disulfide (62.0 g, 0.50 moles) was added. The reaction mixture was heated to 152° C., then heated slowly over a 5 hour period to 180° C., and finally held at 180° C. for an additional 10 hours. Ethyl mercaptan was removed continuously by distillation. The reaction mixture was cooled to 100° C., then vacuum distilled at 100 mm mercury until the pot temperature reached 200° C. to give 70.8 g of distillate. GC analysis indicated the distillate contained 34.0 g of ortho-(ethylthio)phenol (44% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04599451 |
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| Quelldatensatz | uspto-grants-1986_07 |
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| ORD ID | ord-50a7b65bcbe74258a579152409d7003f |
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| Quellennotiz | uspto-grants-1986_07 |
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