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
- 70 °C
PROCEDURE
实验过程
2-Amino-3-nitrophenol B1 (5 g; 32.4 mmol) was dissolved in concentrated HCl (75 mL) and 1,4-dioxane (14.7 mL). The mixture was heated to 70° C. until most of the solids were in solution. The reaction mixture was cooled to 0° C. (ice bath), and sodium nitrite (2.23 g; 32.3 mmol) in H2O (5.4 mL) was added over a period of 3 hours to the brown solution. The temperature was maintained below 10° C. during the addition and the stirring was continued for an additional 15 min at 0° C. This diazonium intermediate was poured into a solution of Cu(I)Cl (3.8 g; 38.9 mmol) in H2O (18.5 mL) and conc. HCl (18.5 mL) at 0° C. The reaction was stirred for 15 min at 0° C., warmed to 60° C., and stirred for an additional 15 min The reaction mixture was then brought to room temperature, and left to stir overnight. The reaction mixture was transferred to a separatory funnel and extracted with ether (3×150 mL). The organic layers were combined, washed with brine (1×), dried (Na2SO4), filtered and concentrated to afford the crude product (5.83 g) as a red-brown oil. The crude material was purified by flash column chromatography (1:25 ultra pure silica gel, 230-400 mesh, 40-60 mm, 60 angstroms; 3:1 hexane/EtOAc as the solvent) to afford pure 2-chloro-3-nitrophenol C2 (48%; 2.7 g) as an orange solid. MS 171.8 (MH)−: Homogeneity by HPLC (TFA) @ 220 nm: 96%.
WORKUP
后处理
- additionwas added over a period of 3 hours to the brown solution
- temperatureThe temperature was maintained below 10° C. during the addition
- temperaturewarmed to 60° C.
- stirringstirred for an additional 15 min The reaction mixture
- customwas then brought to room temperature
- waitleft
- stirringto stir overnight
- customThe reaction mixture was transferred to a separatory funnel
- extractionextracted with ether (3×150 mL)
- washwashed with brine (1×)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customto afford the crude product (5.83 g) as a red-brown oil
- customThe crude material was purified by flash column chromatography (1:25 ultra pure silica gel, 230-400 mesh, 40-60 mm, 60 angstroms