反応 #409808
ord-5ec09a140fd646e69f708d2feb3bb2e7
反応方程式
試薬
反応条件
後処理
- 1その他4-Oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylic acid is prepared
- 2温度then cooled in an ice water bath
- 3workup.ADDITIONis added dropwise to the cold
- 4その他to reach ambient temperature
- 5温度While cooling the reaction mixture via a water bath
- 6workup.STIRRINGAfter stirring at ambient temperature for 15.5 h
- 7温度the reaction mixture is cooled in an ice water bath
- 8濃縮The reaction mixture is concentrated in vacuo, 1 L of ice
- 9workup.ADDITIONis added
- 10ろ過the precipitate filtered
- 11洗浄washed with ice water (3×200 mL)
- 12その他dried in a vacuum oven at 75° C.
実験手順
4-Oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylic acid is prepared according to the following procedure. Potassium hydroxide (345 g, 6.15 mol) is dissolved in methyl alcohol (1.2 L) then cooled in an ice water bath. A solution of cyclohexanedione (714 g, 6.15 mol) in methyl alcohol (1.2 L), dissolved using gentle heat, is added dropwise to the cold, stirred KOH solution over 2 h. A solution of ethyl bromopyruvate (1200 g, 6.15 mol) in methyl alcohol (1.5 L) is then added dropwise over 3 h. The reaction mixture is allowed to reach ambient temperature and stirred an additional 14.5 h. While cooling the reaction mixture via a water bath, a solution of sodium hydroxide (492 g, 12.4 mol) in water (984 mL) is added dropwise over 2.5 h. After stirring at ambient temperature for 15.5 h, the reaction mixture is cooled in an ice water bath, 500 g of ice added, and the resulting mixture is then acidified with concentrated hydrochloric acid (ca 1 L) to pH 1. The reaction mixture is concentrated in vacuo, 1 L of ice is added, and the precipitate filtered, washed with ice water (3×200 mL), and then dried in a vacuum oven at 75° C. to afford 4-oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylic acid (560 g). m.p. 137-138° C.