反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 92.5 °C
PROCEDURE
实验过程
To a mixture of 5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde (3.00 g), malonic acid (1.99 g) and bis(2-methoxyethyl) ether (9 mL) was added dropwise piperidine (1.89 mL) over about 10 min. The mixture was stirred at 90-95° C. for 1 hr. and further at 105-110° C. for 4 hrs. After cooling to 25° C., toluene (12 mL) and 1N aqueous sodium hydroxide solution (15 mL) were added and the mixture was stirred. The aqueous layer was separated and the organic layer was extracted with 1N aqueous sodium hydroxide solution (6 mL). The aqueous layers were combined and washed with toluene. The layers were adjusted to pH 3.5-4.0 with 2N hydrochloric acid at 20-30° C. and water (9 mL) was added dropwise. After stirring at 25° C. for 1 hr., the precipitated crystals were collected by filtration and washed with 20% ethanol to give (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acid (3.24 g, yield 90%).
WORKUP
后处理
- waitand further at 105-110° C. for 4 hrs
- temperatureAfter cooling to 25° C.
- stirringthe mixture was stirred
- customThe aqueous layer was separated
- extractionthe organic layer was extracted with 1N aqueous sodium hydroxide solution (6 mL)
- washwashed with toluene
- customwere adjusted to pH 3.5-4.0 with 2N hydrochloric acid at 20-30° C.
- additionwater (9 mL) was added dropwise
- stirringAfter stirring at 25° C. for 1 hr
- filtration, the precipitated crystals were collected by filtration
- washwashed with 20% ethanol