HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1877076Erstellt: 26. Oktober 2026
Hydrochloric Acid → 1,4-Dioxaspiro[4.5]dec-8-yl(2-methyl-5-phenylfuran-3-yl)methanol
https://huagongshe.com/reaction/1877076
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | 2-Methyl-5-phenyl-3-furaldehyde | HCID 2795313 | — |
| Edukt | HCID 178420630 | HCID 178420630 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1,4-Dioxaspiro[4.5]dec-8-yl(2-methyl-5-phenylfuran-3-yl)methanol | HCID 68511110 | 91% |
Reaktionsschritte
To a solution of 2-methyl-5-phenylfuran-3-carbaldehyde (2.4 g) in tetrahydrofuran (30 mL) was added dropwise 0.4N bromo(1,4-dioxaspiro[4.5]dec-8-yl)magnesium-tetrahydrofuran solution (33.5 mL) at 0° C. and, after the completion of the dropwise addition, the mixture was stirred at 0° C. for 1 hr. The reaction mixture was treated with 1N hydrochloric acid, poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column (0% ethyl acetate/hexane to 30% ethyl acetate/hexane) to give the title compound (3.9 g, 91%) as a yellow crystal.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08309580B2 |
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| Quelldatensatz | uspto-grants-2012_11 |
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| ORD ID | ord-ce0fe931b60c439dac559fca343f0011 |
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| Quellennotiz | uspto-grants-2012_11 |
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