1-(2-Hydroxyethyl)-1H-pyrazole → 2-(2-(1H-pyrazol-1-yl)ethoxy)-6-nitrobenzonitrile
Reaction equation
[N:1]1([CH2:6][CH2:7][OH:8])[CH:5]=[CH:4][CH:3]=[N:2]1.[N+:9]([C:12]1[CH:19]=[CH:18][CH:17]=[C:16]([N+]([O-])=O)[C:13]=1[C:14]#[N:15])([O-:11])=[O:10]>>[N:1]1([CH2:6][CH2:7][O:8][C:16]2[CH:17]=[CH:18][CH:19]=[C:12]([N+:9]([O-:11])=[O:10])[C:13]=2[C:14]#[N:15])[CH:5]=[CH:4][CH:3]=[N:2]1Participants
3
Procedure
Prepared as in Example 215c from 2-(1H-pyrazol-1-yl)ethanol and 2,6-dinitrobenzonitrile in 89.2% yield. MS 259 (MH+).
Sources & evidence
- ORD record
- ord-745e63126d9b4cd8ae7655d285788c4f
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09181276B2
Reaction notes
Loading…