Hydrochloric Acid → HCID 19990532, compound
Reaction equation
[CH2:1]([C:5]1([CH2:27][CH2:28][CH2:29][CH3:30])[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[O:14][CH2:15][C:16]2[CH:25]=[CH:24][C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[N:17]=2)[C:6]1=[O:26])[CH2:2][CH2:3][CH3:4].[ClH:31]>C(OCC)C>[ClH:31].[CH2:1]([C:5]1([CH2:27][CH2:28][CH2:29][CH3:30])[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[O:14][CH2:15][C:16]2[CH:25]=[CH:24][C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[N:17]=2)[C:6]1=[O:26])[CH2:2][CH2:3][CH3:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2,2-Dibutyl-4-(2-quinolylmethoxy)-1-indanone hydrochloride was prepared by treating 2,2-dibutyl-4-(2-quinolylmethoxy)-1-indanone with hydrogen chloride in ethyl ether.
Sources & evidence
- ORD record
- ord-8b884054843946ff846c889d8247ac21
- Source dataset
- uspto-grants-1990_10
- Patent number
- US04965274
Reaction notes
Loading…