Ethanol hydrochloride → HCID 136351074, compound
Reaction equation
[OH:1][C:2]1[C:9]([O:10][CH2:11][CH2:12][O:13][CH2:14][CH2:15][O:16][CH3:17])=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:5].[CH3:18][CH2:19][OH:20].[ClH:21]>>[ClH:21].[OH:1][C:2]1[C:9]([O:10][CH2:11][CH2:12][O:13][CH2:14][CH2:15][O:16][CH3:17])=[CH:8][CH:7]=[CH:6][C:3]=1[C:4](=[NH:5])[O:20][CH2:19][CH3:18]Participants
3
Procedure
A solution of 2-hydroxy-3-(2-(2-methoxyethoxy)ethoxy)benzonitrile (6 g) in EtOH/HCl (g) (150 mL) was heated to 40° C. overnight in a sealed tube. The solvent was evaporated under vacuum and the residue (7 g, crude) was used for the next step without further purification.
Workup
- customThe solvent was evaporated under vacuum
- customthe residue (7 g, crude) was used for the next step without further purification
Sources & evidence
- ORD record
- ord-f4064b5af8634a8d83c77c9e1cbd28a0
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09045440B2
Reaction notes
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