HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 746197Erstellt: 25. Oktober 2026
Methyl iodide → P-tert-Butoxy-alpha-methyl styrene
https://huagongshe.com/reaction/746197
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | tert-Butyl peroxybenzoate | HCID 11966 | — |
| Edukt | 4-Chloro-alpha-methylstyrene | HCID 74381 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Edukt | 4,4'-Diisopropenylbiphenyl | HCID 13422373 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | P-tert-Butoxy-alpha-methyl styrene | HCID 11206291 | 69,3% |
Reaktionsschritte
The procedure of Example 1 was repeated, except that there was utilized 16.9 grams (0.70 mole) of magnesium metal and 100 grams (0.66 mole) of 4-chloro-α-methylstyrene dissolved in 200 ml. of tetrahydrofuran. The Grignard reaction was started by the addition of a small amount of methyl iodide. After the reaction mixture had been refluxed for 12 hours, there was added at 0° C. in a dropwise manner a solution of 85 grams of t-butylperbenzoate in 300 ml. of ethylether. A crystalline product identified as 4,4'-diisopropenylbiphenyl was isolated from the oil which was recovered by filtering the mixture and washing with methanol. After stripping the methanol, a 69.3% yield of 4-t-butoxy-α-methylstyrene was isolated by fractional distillation as a colorless liquid having a boiling point of 65°-68° C. at 0.03 millimeters.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04603101 |
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| Quelldatensatz | uspto-grants-1986_07 |
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| ORD ID | ord-63997216ebee447ba405a25cc1993547 |
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| Quellennotiz | uspto-grants-1986_07 |
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