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
- 110 °C
PROCEDURE
实验过程
A mixture of 4-bromo-5-fluoro-2-hydrazinylbenzoic acid hydrochloride (5.37 g, 18.8 mmol), ethyl 3-oxocyclohexanecarboxylate (3.52 g, 20.7 mmol) and acetic acid (3.23 mL, 56.4 mmol) in toluene (90 mL) was heated at 110° C. for 20 h. The solvent was removed under reduced pressure, and the residue was diluted with toluene (43 mL) and trifluoroacetic acid (11 mL). The mixture was stirred at 90-94° C. overnight. The cooled mixture was diluted with EtOAc, sonicated, and the precipitate was collected by filtration. The filtrate was concentrated and resuspended in EtOAc with sonication, resulting in another precipitate which was also collected by filtration and washed with EtOAc. The combined solids were triturated twice with MeOH to give a solid. The combined filtrates were concentrated and the residue was triturated with MeOH to give additional solid. The solids were combined to give 5-bromo-2-ethoxycarbonyl-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid as a pale yellow solid (3.38 g). Mass spectrum m/z 384, 386 (M+H)+.
WORKUP
后处理
- customThe solvent was removed under reduced pressure
- additionthe residue was diluted with toluene (43 mL) and trifluoroacetic acid (11 mL)
- additionThe cooled mixture was diluted with EtOAc
- customsonicated
- filtrationthe precipitate was collected by filtration
- concentrationThe filtrate was concentrated
- customresuspended in EtOAc with sonication
- customresulting in another precipitate which
- filtrationwas also collected by filtration
- washwashed with EtOAc
- customThe combined solids were triturated twice with MeOH
- customto give a solid
- concentrationThe combined filtrates were concentrated
- customthe residue was triturated with MeOH
- customto give additional solid