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HRID 481851作成日:2026年10月27日

Methyl acetoacetate → 5,6-Dihydro-4-hydroxy-6-phenyl-6-propyl-2H-pyran-2-one

https://huagongshe.com/reaction/481851

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl acetoacetateHCID 7757—
反応物ButyrophenoneHCID 10315—
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物5,6-Dihydro-4-hydroxy-6-phenyl-6-propyl-2H-pyran-2-oneHCID 54708006—

反応条件

温度0 °C

反応手順

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) δ0.88 (t, 3H), 1.1-1.4 (m, 2H), 1.95 (m, 2H), 2.90 (d, 1H), 2.92 (d, 1H), 3.25 (d, 1H), 3.35 (d, 1H), 7.2-7.4 (m, 5H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05789440
出典データセットuspto-grants-1998_08
ORD IDord-adb45a93712b42b5979aca8328a8e04b
出典メモuspto-grants-1998_08