Hydrochloric Acid → HCID 13287881, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4](/[CH:14]=[CH:15]/[C:16]([O:18]CC)=[O:17])[CH:5]=[CH:6][C:7]=1[CH2:8][N:9]1[CH:13]=[CH:12][N:11]=[CH:10]1.Cl>>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4](/[CH:14]=[CH:15]/[C:16]([OH:18])=[O:17])[CH:5]=[CH:6][C:7]=1[CH2:8][N:9]1[CH:13]=[CH:12][N:11]=[CH:10]1Participants
3
Procedure
A mixture of ethyl (E)-3-[3-chloro-4-(imidazol-1-ylmethyl)phenyl]prop-2-enoate (0.1 g, 0.31 mmol) and hydrochloric acid (6M, 2.0 ml) was stirred and boiled for 2 h. The reaction mixture was then concentrated under reduced pressure, when ethanol (4.0 ml) was added and the reaction mixture was again concentrated.
Workup
- concentrationThe reaction mixture was then concentrated under reduced pressure, when ethanol (4.0 ml)
- additionwas added
- concentrationthe reaction mixture was again concentrated
Sources & evidence
- ORD record
- ord-b7b67fad2e844a39959b4989766e5833
- Source dataset
- uspto-grants-1985_12
- Patent number
- US04562199
Reaction notes
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