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
- 90 °C
PROCEDURE
实验过程
To a suspension of hydroxylamine hydrochloride (351 mg, 5.05 mmol) in 4 ml EtOH was added 1.86 ml 21% wt sodium ethoxide in ethanol. The resulting mixture was stirred for 10 min at r.t. before addition of 3-cyano-1-methylpyrazole (40) (535 mg, 5 mmol). The resulting suspension was heated overnight at 90° C. After cooling down, the reaction mixture was diluted with EA then washed with brine. Org. phase was concentrated to dryness to give 506 mg crude intermediate 41. A mixture of the above crude intermediate 41, trifluoromethanesulfonic acid Ytterbium (III) salt (22 mg, 1% mol) and trimethyl orthoacetate (550 μl, 1.2 eq.) in 5 ml EtOH was heated at 85° C. for 2 h. After cooling down to r.t., fine needles formed. After filtration and wash with MeOH 166 mg intermediate 41 was recovered as pale yellow needles. The filtrate was concentrated, subjected to silica gel column purification using 0-100% B (A: hexane; B: EA) to furnish 230 mg 5-methyl-3-(1-methylpyrazol-3-yl)-1,2,4-oxadiazole (42) as white solid.
WORKUP
后处理
- additionwas added 1.86 ml 21%
- temperatureAfter cooling down
- washthen washed with brine
- concentrationphase was concentrated to dryness
- customto give 506 mg crude intermediate 41
- temperaturewas heated at 85° C. for 2 h
- temperatureAfter cooling down to r.t.
- customfine needles formed
- filtrationAfter filtration
- washwash with MeOH 166 mg intermediate 41
- customwas recovered as pale yellow needles
- concentrationThe filtrate was concentrated
- customsubjected to silica gel column purification