4-Aminobenzoic Acid → 4-(cyclohex-3-ene-1-carbonylamino)benzoic Acid
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([C:17](Cl)=[O:18])[CH2:16][CH2:15][CH:14]=[CH:13][CH2:12]1>>[CH:11]1([C:17]([NH:1][C:2]2[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=2)=[O:18])[CH2:16][CH2:15][CH:14]=[CH:13][CH2:12]1Participants
3
Procedure
4-(3-Cyclohexene-1-carbonylamino)-benzoic acid was prepared as described in Example 3 from 12 g (0.0875 mol) of p-aminobenzoic acid and 13.9 g (0.0963 mol) of 3-cyclohexene-1-carboxylic acid chloride.
Sources & evidence
- ORD record
- ord-7ce11b679f6244f7be80aa7da480e088
- Source dataset
- uspto-grants-1977_01
- Patent number
- US04001218
Reaction notes
Loading…