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HRID 22488Erstellt: 25. Oktober 2026
Hexane → 2-Methoxy-5-(3,4,5-trimethoxyphenyl)oxolane
https://huagongshe.com/reaction/22488
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hexane | HCID 8058 | — |
| Edukt | 5-Bromo-1,2,3-trimethoxybenzene | HCID 75885 | — |
| Edukt | Magnesium Bromide | HCID 82241 | — |
| Edukt | 2-(Benzenesulfonyl)-5-methoxyoxolane | HCID 19930462 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Katalysator | Zinc bromide | HCID 10421208 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Methoxy-5-(3,4,5-trimethoxyphenyl)oxolane | HCID 19930459 | 27,3% |
Reaktionsschritte
To stirred solution of 1-bromo-3,4,5-trimethoxybenzene (2.47 g, 10 mmol) in THF (20 ml) at -78° C. was added 2.5M n-butyllithium in hexane (4.4 ml, 11 mmol). After 0.75 h the solution was cannulated into a mixture of 1M zinc(II) bromide in THF (11 ml, 11 mmol) and magnesium(II) bromide etherate (2.86 g, 15 mmol) in THF (10 ml) at -78° C. The resulting mixture was allowed to warm to room temperature over 1 h and then sonicated for 0.4 h. A solution of 2-benzenesulphonyl-5-methoxytetrahydrofuran (1.85 g, 7.5 mmol) in THF (10 ml)was added and the mixture stirred at room temperature for 1 h, sonicated for 1 h and stirred overnight. The reaction was quenched by the addition of aqueous ammonium chloride (20 ml). Work up and purification as described for Example 1(b) gave 2-(3,4,5-trimethoxyphenyl)-5 -methoxytetrahydrofuran (0.55 g, 27%) as a colourless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05428168 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-ab76418b248b473985be7ed447798f4b |
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| Quellennotiz | uspto-grants-1995_06 |
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