4-Aminobenzoic Acid → HCID 837284, compound
Reaction equation
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[CH:11]1([CH2:16][CH2:17][C:18](Cl)=[O:19])[CH2:15][CH2:14][CH2:13][CH2:12]1>>[CH:11]1([CH2:16][CH2:17][C:18]([NH:1][C:2]2[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=2)=[O:19])[CH2:15][CH2:14][CH2:13][CH2:12]1Participants
3
Procedure
4-(3-Cyclopentylpropionylamino)-benzoic acid was prepared as described in Example 3 from 9.63 g (0.07 mol) of p-aminobenzoic acid and 12.4 g (0.077 mol) of 3-cyclopentylpropionyl chloride.
Sources & evidence
- ORD record
- ord-c301d27267c74a3098ceb97e998eee30
- Source dataset
- uspto-grants-1977_01
- Patent number
- US04001218
Reaction notes
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