HCID 57582493, compound → HCID 15980989, compound

HRID 2370469Notes

Reaction equation

HRID 2370469 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

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

  1. temperaturethe mixture cooled
  2. concentrationthen concentrated in vacuo
  3. customThe residual oil was then purified by silica column chromatography (20-40% methanol in CH2Cl2 eluent)

Sources & evidence

ORD record
ord-221fc4d71560423aac1926632b703852
Source dataset
uspto-grants-2014_04
Patent number
US08710100B2

Reaction notes

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