反应 #1267669
ord-d4ab56554a9443c5b1e6120afc9619cf
反应方程式
试剂
反应条件
后处理
- 1其他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其他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浓缩The reaction mixture is concentrated in vacuo, 1L of ice
- 9workup.ADDITIONis added
- 10过滤the precipitate filtered
- 11洗涤washed with ice water (3×200 mL)
- 12其他dried in a vacuum oven at 75° C.
实验过程
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 1L) to pH 1. The reaction mixture is concentrated in vacuo, 1L 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.