Hydrochloric Acid → HCID 86688757, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:28])[CH2:4][O:5][C:6]1[CH:10]=[C:9]([CH3:11])[N:8]([CH2:12][C:13]2[CH:18]=[C:17]([Cl:19])[CH:16]=[CH:15][C:14]=2[O:20]CC2C=CC=CC=2)[N:7]=1.Cl>CO.O=[Pt]=O>[CH3:1][O:2][C:3](=[O:28])[CH2:4][O:5][C:6]1[CH:10]=[C:9]([CH3:11])[N:8]([CH2:12][C:13]2[CH:18]=[C:17]([Cl:19])[CH:16]=[CH:15][C:14]=2[OH:20])[N:7]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of [1-(2-benzyloxy-5-chloro-benzyl)-5-methyl-1H-pyrazol-3-yloxy]-acetic acid methyl ester, 8, (1.19 g, 2.97 mmol), PtO2 (0.17 g) and conc. HCl (2 ml) in MeOH was stirred under a H2 atmosphere for 3 hours. The catalyst was removed by filtration, the volatiles were removed in vacuo and the crude product was purified on silica to yield [1-(5-chloro-2-hydroxy-benzyl)-5-methyl-1H-pyrazol-3-yloxy]-acetic acid methyl ester, 9.
Workup
- customThe catalyst was removed by filtration
- customthe volatiles were removed in vacuo
- customthe crude product was purified on silica
Sources & evidence
- ORD record
- ord-03529796b6b0493ca4ce85a7c8fc3c96
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08969589B2
Reaction notes
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