Methanol → 1-Methyl-3,5-diphenylpyrazole

HRID 357531

Reaction equation

HRID 357531 reaction equation
[C:1]1([C:7]2[CH:11]=[C:10]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)[NH:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(OC)(O[CH3:22])(=O)=O.CO>>[CH3:22][N:8]1[C:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[CH:11][C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[N:9]1

Participants

4

Conditions

Temperature
200 °C

Procedure

As in Example 2, a melt consisting of 10 g (0.0455 mol) of 3,5-diphenylpyrazole and 0.057 g (0.00455 mol) of dimethyl sulfate was prepared at 200° C. Over the course of 5 hours, 435 g (13.6 mol) of methanol were vaporized at 155° C. and passed through the melt which was maintained at 200° C. 10.4 g (96.9%) of 1-methyl-3,5-diphenylpyrazole were obtained, boiling point 190° C./3 mbar, with a content of 99.2% (GC).

Workup

  1. customwas prepared at 200° C
  2. customwere vaporized at 155° C.

Sources & evidence

ORD record
ord-18b6bab8692a46d8a76e110c784769e9
Source dataset
uspto-grants-1998_11
Patent number
US05840913

Linked notes

Loading…