4-Aminobenzoic Acid → HCID 21486329, compound

HRID 1414193Notes

Reaction equation

HRID 1414193 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:18](Cl)=[O:19])[CH2:17][CH2:16][CH:15]=[CH:14][CH2:13][CH2:12]1>>[CH:11]1([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])[CH2:17][CH2:16][CH:15]=[CH:14][CH2:13][CH2:12]1

Participants

3

Reactant 2

HCID 9784-Aminobenzoic AcidHCID 12430217HCID 12430217, compound

Product 1

HCID 21486329HCID 21486329, compound

Procedure

4-(4-Cycloheptene-1-carbonylamino)-benzoic acid was prepared as described in Example 3 from 4.45 g (0.0324 mol) of p-aminobenzoic acid and 5.7 g (0.0359 mol) of 4-cycloheptene-1-carboxylic acid chloride.

Sources & evidence

ORD record
ord-9542131e5eb04655b2f8bf20ffaabc0f
Source dataset
uspto-grants-1977_01
Patent number
US04001218

Reaction notes

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