Adipic Acid → HCID 86733666, compound
Reaction equation
[C:1]([OH:10])(=[O:9])[CH2:2][CH2:3][CH2:4][CH2:5][C:6]([OH:8])=[O:7].[C:11]1([N:17]=[N:18][C:19]2[CH:24]=[CH:23][C:22](O)=[CH:21][CH:20]=2)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>C(Cl)(Cl)Cl>[C:11]1([N:17]=[N:18][C:19]2[CH:24]=[CH:23][C:22]([O:7][C:6](=[O:8])[CH2:5][CH2:4][CH2:3][CH2:2][C:1]([O:10][C:22]3[CH:21]=[CH:20][C:19]([N:18]=[N:17][C:11]4[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=4)=[CH:24][CH:23]=3)=[O:9])=[CH:21][CH:20]=2)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
164 g. of polyphosphoric acid ethyl ester is dissolved in 60 ml. of chloroform. A suspension of 14.86 g. of adipic acid and 40.0 g. of p-(phenylazo)-phenol in 340 ml. of chloroform is added to this solution. The reaction mixture is agitated for 4 hours. Then, 35 g. of adipic acid bis(4-phenylazophenyl)ester is obtained by vacuum-filtering the reaction mixture; this product is recrystallized from ethyl acetate. In this way, 30 g. of a pure compound is obtained, m.p. 176°-177° C.
Workup
- additionA suspension of 14.86 g
Sources & evidence
- ORD record
- ord-95ae36b9e93841f68e9fc3b08f8dc15b
- Source dataset
- uspto-grants-1976_07
- Patent number
- US03968219
Reaction notes
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