HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 347849Erstellt: 24. Oktober 2026
Triisopropyl borate → 2,6-Dimethoxy-4-methoxymethylphenylboric acid
https://huagongshe.com/de/reaction/347849
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triisopropyl borate | HCID 21531 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 3,5-Dimethoxy(methoxymethyl)benzene | HCID 10329976 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2,6-Dimethoxy-4-methoxymethylphenylboric acid | HCID 23080945 | — |
Reaktionsschritte
To a solution of 3,5-dimethoxy(methoxymethyl)benzene (23.7 g) in tetrahydrofuran (500 mL) was added n-butyllithium (1.56M hexane solution; 100 mL) at −78° C., and the reaction mixture was stirred for 30 minutes while cooling with ice. After cooling the internal temperature of the obtained reaction mixture to −78° C., to a reaction mixture was added triisopropoxyborane (39 mL), and the internal temperature was raised to room temperature while stirring. After completion of the reaction, saturated aqueous ammonium chloride was added to the reaction mixture while cooling with ice, and then ethyl acetate was added to the reaction mixture, the organic extract was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography and the title compound (7.5 g) was obtained as a yellow oil from the ethyl acetate fraction.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07176216B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-a0ecb90d07af4a3f8329a3cbccacfce1 |
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| Quellennotiz | uspto-grants-2007_02 |
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