反应 #1340630

反应方程式

methyl (5-hydroxy-1-methyl-1H-pyrazol-3-yl)acetate

methyl[1-(2-chlorophenyl)-5-hydroxy-1H-pyrazol-3-yl]acetate

acetic acid

BuC(OEt)3

→

methyl[(4Z)-4-(1-ethoxypentylidene)-1-methyl-5-oxo-4,5-dihydro-1H-pyrazol-3-yl]acetate

溶剂

acetonitrile

反应条件

后处理

1. 1
   workup.ADDITIONThe mixture of the
2. 2
   浓缩The resulting red solution was concentrated in vacuo
3. 3
   其他to afford a red syrup that
4. 4
   洗涤was washed with cyclohexane
5. 5
   其他dried in vacuo
6. 6
   其他Due to its relative instability, no further purification of methyl[(4Z)-4-(1-ethoxypentylidene)-1-methyl-5-oxo-4,5-dihydro-1H-pyrazol-3-yl]acetate

实验过程

The mixture of the above obtained methyl (5-hydroxy-1-methyl-1H-pyrazol-3-yl)acetate (Compound of Formula (IV), 0.80 g) in acetonitrile (5 mL), glacial acetic acid (21 μl 0.1 equiv.) and BuC(OEt)3 (3 eq.) was heated at 70° C. for 1 h 15. The resulting red solution was concentrated in vacuo to afford a red syrup that was washed with cyclohexane and then dried in vacuo. Due to its relative instability, no further purification of methyl[(4Z)-4-(1-ethoxypentylidene)-1-methyl-5-oxo-4,5-dihydro-1H-pyrazol-3-yl]acetate was conducted (1.0 g, quantitative yield). MS (ESI+): 283.4; MS (ESI−): 281.3.

来源