HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 357817Erstellt: 25. Oktober 2026
Methyl acetoacetate → 5,6-Dihydro-4-hydroxy-6-phenyl-6-propyl-2H-pyran-2-one
https://huagongshe.com/reaction/357817
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl acetoacetate | HCID 7757 | — |
| Edukt | Butyrophenone | HCID 10315 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 5,6-Dihydro-4-hydroxy-6-phenyl-6-propyl-2H-pyran-2-one | HCID 54708006 | — |
Reaktionsschritte
The title compound was prepared as described in the General Method 1 using 5 mmol of methyl acetoacetate, 5.5 mmol of NaH 60% dispersion in oil, 5.5 mmol of 1.6M n-butyl lithium in hexane, 5.5 mmol of butyrophenone and 14 mL of tetrahydrofuran. After addition of the ketone, the reaction was stirred for 90 minutes at 0° C. The reaction was poured into saturated NH4Cl solution and extracted with ethyl acetate. The organic layer was dried over MgSO4, concentrated, and the residue flash chromatographed using hexane/ethyl acetate 80/20 as eluent. The aldol product was stirred at room temperature in 100 mL of 0.1N NaOH for 3.5 hours. The reaction was worked up as in General Method 1 and the product triturated from diethyl ether to afford a solid (m.p. 131.5°-132° C.). 1H NMR (CDCl3) δ 0.88 (t, 3 H), 1.1-1.4 (m, 2 H), 1.95 (m, 2 H), 2.90 (d, 1 H), 2.92 (d, 1 H), 3.25 (d, 1 H), 3.35 (d, 1 H), 7.2-7.4 (m, 5 H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05840751 |
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| Quelldatensatz | uspto-grants-1998_11 |
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| ORD ID | ord-5286afc3703040f7bdf4413b156c16c7 |
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| Quellennotiz | uspto-grants-1998_11 |
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