تفاعل #1340630

ord-8ddae73c475047ca9904455e40b28531

معادلة التفاعل

COC(=O)Cc1cc(O)n(-c2ccccc2Cl)n1
methyl (5-hydroxy-1-methyl-1H-pyrazol-3-yl)acetate
COC(=O)Cc1cc(O)n(-c2ccccc2Cl)n1
methyl[1-(2-chlorophenyl)-5-hydroxy-1H-pyrazol-3-yl]acetate
CC(=O)O
acetic acid
CCCCC(OCC)(OCC)OCC
BuC(OEt)3
CCCC/C(OCC)=C1/C(=O)N(C)N=C1CC(=O)OC
methyl[(4Z)-4-(1-ethoxypentylidene)-1-methyl-5-oxo-4,5-dihydro-1H-pyrazol-3-yl]acetate

المذيبات

ظروف التفاعل

درجة الحرارة
70°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONThe mixture of the
  2. 2
    تركيزThe resulting red solution was concentrated in vacuo
  3. 3
    أخرىto afford a red syrup that
  4. 4
    غسيلwas washed with cyclohexane
  5. 5
    أخرىdried in vacuo
  6. 6
    أخرىDue 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

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08455485B2uspto-grants-2013_06