Hydrochloric Acid → HCID 70478180, compound
Reaction equation
C([O:3][C:4](=[O:19])[CH2:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([CH2:13][C:14]2[NH:15][CH:16]=[CH:17][N:18]=2)[CH:8]=1)C.[ClH:20]>C(#N)C>[ClH:20].[NH:15]1[CH:16]=[CH:17][N:18]=[C:14]1[CH2:13][C:9]1[CH:8]=[C:7]([CH:12]=[CH:11][CH:10]=1)[O:6][CH2:5][C:4]([OH:19])=[O:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Hydrolysis of 3-(1-imidazolylmethyl)phenoxyacetic acid ethyl ester free base with concentrated hydrochloric acid according to the method of Example 7 gave 3-(1-imidazolylmethyl)phenoxyacetic acid hydrochloride, m.p. 179°-181° C. (from aqueous acetonitrile). Found: C, 52.23, H, 4.84, N, 10.65. C12H12N2O3.HCl requires: C, 53.64, H, 4.88, N, 10.43%.
Sources & evidence
- ORD record
- ord-70d55c8885474793a020a01aff58d46a
- Source dataset
- uspto-grants-1984_05
- Patent number
- US04448781
Reaction notes
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