Hydrochloric Acid → Benzenecarboximidic acid, 3-acetyl-, ethyl ester, hydrochloride
Reaction equation
[C:1]([C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][CH:11]=1)[C:7]#[N:8])(=[O:3])[CH3:2].[ClH:12].[CH3:13][CH2:14][O:15]CC>C(O)C>[ClH:12].[CH2:14]([O:15][C:7](=[NH:8])[C:6]1[CH:9]=[CH:10][CH:11]=[C:4]([C:1](=[O:3])[CH3:2])[CH:5]=1)[CH3:13]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 7.25 g (0.05 mol) of 3-acetylbenzonitrile in 150 ml of ether and 4.5 ml of ethanol is saturated at 0° with dry hydrochloric acid gas and then left to stand at 0° for 2 days. The product which crystallises out is filtered off and recrystallised from ethanol/ether; m.p. 110° (with decomposition).
Workup
- waitleft
- customThe product which crystallises out
- filtrationis filtered off
- customrecrystallised from ethanol/ether
Sources & evidence
- ORD record
- ord-0ae894ec146142b3a01059ae9694846f
- Source dataset
- uspto-grants-1993_08
- Patent number
- US05238941
Reaction notes
Loading…