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HRID 2163261作成日:2026年10月25日

Potassium Hydroxide → 2-Hydroxymethyl-3-(5-carboethoxypentyloxy)-4-pyrone

https://huagongshe.com/reaction/2163261

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物3-hydroxy-2-(hydroxymethyl)-4H-pyran-4-oneHCID 9869622—
反応物Ethyl 6-iodohexanoateHCID 10880140—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物2-Hydroxymethyl-3-(5-carboethoxypentyloxy)-4-pyroneHCID 2334485554%

反応手順

To a solution of 2.75 g (0.042 mole) of potassium hydroxide in 38 ml of ethanol and 10 ml of water was added 5.93 g (0.042 mole) of 2-hydroxymethyl-3-hydroxy-4-pyrone, and the resulting mixture heated to 50°. A 12.4 g (0.046 mole) portion of ethyl 6-iodohexanoate was then added and the resulting clear solution heated at reflux for 7 hr under a nitrogen atomsphere. Removal of the ethanol under reduced pressure left a residue which was dissolved in methylene chloride. The organic solution was washed successively with aqueous NaHCO3 and saturated brine, was dried over magnesium sulfate, and was evaporated to afford a viscous oil. This material was chromatographed on silica gel eluting with ethyl acetate to give 6.34 g (54%) of oily product, 2-hydroxymethyl-3-(5-carboethoxypentyloxy)-4-pyrone: NMR (CDCl3): δ1.22 (3H, t, J = 7Hz), 2.30 (2H, t, J = 5.5 Hz), 4.63 (2H, s), 6.35 (1H, d, J = 6 Hz), 7.73 (1H, d, J = 6 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04132847
出典データセットuspto-grants-1979_01
ORD IDord-c5639ed8186d4c33b3e3c914a0c3f87e
出典メモuspto-grants-1979_01