4-Aminobenzoic Acid → HCID 888179, compound

HRID 1414189Notes

Reaction equation

HRID 1414189 reaction equation
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[CH2:11]1[CH2:16][CH2:15][CH2:14][CH:13]([CH2:17][CH2:18][C:19](Cl)=[O:20])[CH2:12]1>>[CH2:11]1[CH2:16][CH2:15][CH2:14][CH:13]([CH2:17][CH2:18][C:19]([NH:1][C:2]2[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=2)=[O:20])[CH2:12]1

Participants

3

Reactant 2

HCID 9784-Aminobenzoic AcidHCID 2734098Cyclohexylpropionyl chloride

Product 1

HCID 888179HCID 888179, compound

Procedure

4-(3-Cyclohexanepropionylamino)-benzoic acid was prepared as described in Example 3 from 10.0 g (0.073 mol) of p-aminobenzoic acid and 14.0 g (0.08 mol) of 3-cyclohexanepropionyl chloride.

Sources & evidence

ORD record
ord-ee6383b6f66f4ebb8ba7051924676ac6
Source dataset
uspto-grants-1977_01
Patent number
US04001218

Reaction notes

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