Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Piperonyl alcohol | HCID 10322 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 1,3-Benzodioxole, 5-(chloromethyl)- | HCID 88713 | 100% |
Reaktionsschritte
Piperonyl alcohol (10 g, 65.7 mmol) was dissolved in benzene. Triethylamine (11 ml, 78.8 mmol) and thionyl chloride (11 ml, 131.4 mmol) were added dropwise thereto and was stirred for 24 hours at 0° C. The reaction mixture was extracted with sodium bicarbonate and ethyl acetate, the organic layer was separated, and dried over anhydrous magnesium sulfate to obtain 5-chloromethyl benzo[1,3]dioxol (11.2 g, yield 100%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741323B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-d083df6e630e4365a26adb042fc2f702 |
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| Quellennotiz | uspto-grants-2010_06 |
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