4-Aminophenylacetic acid → HCID 16785030, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=[O:10])=[CH:4][CH:3]=1.[CH:12]1([C:16](Cl)=[O:17])[CH2:15][CH2:14][CH2:13]1>>[CH:12]1([C:16]([NH:1][C:2]2[CH:3]=[CH:4][C:5]([CH2:8][C:9]([OH:11])=[O:10])=[CH:6][CH:7]=2)=[O:17])[CH2:15][CH2:14][CH2:13]1Participants
3
Procedure
(4-Cyclobutanecarbonylaminophenyl)-acetic acid was prepared as described in Example 3 from 7.0 g (0.0464 mol) of (p-aminophenyl)-acetic acid and 6.6 g (0.0557 mol) of cyclobutanecarboxylic acid chloride.
Sources & evidence
- ORD record
- ord-3a910d3d8718493ead24ce57e4c8002c
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03931153
Reaction notes
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