Dimethyl acetylenedicarboxylate → Heptylbenzene
Reaction equation
[CH2:1]([C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][C:9]=1[N+:17]([O-:19])=[O:18])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].COC(C#CC(OC)=O)=O>>[CH2:1]([C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][C:9]=1[N+:17]([O-:19])=[O:18])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[CH2:1]([C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7]Participants
4
Procedure
The 2,4-diamino-1-n-heptylbenzene so obtained was used directly for the reaction with acetylene dicarboxylic acid dimethyl ester. The said 1-n-heptyl-2,4-dinitrobenzene was obtained by nitration of n-heptylbenzene in a similar manner to that described for the nitration of n-pentylbenzene in Example 7.
Sources & evidence
- ORD record
- ord-a857604f839949c496468c8d2a88f21d
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03984551
Reaction notes
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