Reaction equation
Cl[CH2:2][CH2:3][C:4]1[CH:5]=[N:6][N:7]([CH3:9])[CH:8]=1.[CH3:10][NH2:11]>>[CH3:10][NH:11][CH2:2][CH2:3][C:4]1[CH:5]=[N:6][N:7]([CH3:9])[CH:8]=1Participants
3
Procedure
To neat 4-(2-chloroethyl)-1-methyl-1H-pyrazole (50 g, 0.24 mol) was added a 25% aqueous solution of methylamine (1.15 L, 7.21 mol). The mixture was placed into an autoclave at 60° C. for 15 h. The resulting mixture was concentrated in vacuo, treated with aqueous solution of NaOH and extracted with DCM. The combined organic layers were concentrated in vacuo and purified by vacuum distillation to afford the title compound. b.p. 89-90° C./2 mm Hg.
Workup
- concentrationThe resulting mixture was concentrated in vacuo
- additiontreated with aqueous solution of NaOH
- extractionextracted with DCM
- concentrationThe combined organic layers were concentrated in vacuo
- distillationpurified by vacuum distillation
Sources & evidence
- ORD record
- ord-6e4fd895a7144b869cd4b77e9541f4cc
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367706B2
Linked notes
Loading…