HCID 57582493, compound → HCID 15980989, compound
Reaction equation
C([NH:4][C:5]1[CH:10]=[CH:9][C:8]([CH:11]([O:15][CH2:16][CH3:17])[C:12]([OH:14])=[O:13])=[CH:7][CH:6]=1)(=O)C>O.NN>[CH2:16]([O:15][CH:11]([C:8]1[CH:7]=[CH:6][C:5]([NH2:4])=[CH:10][CH:9]=1)[C:12]([OH:14])=[O:13])[CH3:17]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
2-(4-Acetamidophenyl)-2-ethoxyacetic acid (7.54 g, 31.8 mmol) was heated with hydrazine monohydrate (40 ml) for 16 hr, the mixture cooled then concentrated in vacuo The residual oil was then purified by silica column chromatography (20-40% methanol in CH2Cl2 eluent) to give (±)-2-ethoxy-2-(4′-aminophenyl)-acetic acid (2.3 g, 37%) as a white foam.
Workup
- temperaturethe mixture cooled
- concentrationthen concentrated in vacuo The residual oil
- customwas then purified by silica column chromatography (20-40% methanol in CH2Cl2 eluent)
Sources & evidence
- ORD record
- ord-b22695c3aebc41518dfe24f1f5dee668
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09133099B2
Reaction notes
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