HCID 14438868, compound → HCID 14438871, compound

HRID 1110454Notes

Reaction equation

HRID 1110454 reaction equation
[CH3:1][C:2]1C=C(C)C=CC=1S(CCC)(=O)=O.[CH3:15][C:16]1[C:21]([N+:22]([O-:24])=[O:23])=[C:20]([CH3:25])[C:19]([S:26]([CH3:29])(=[O:28])=[O:27])=[CH:18][C:17]=1[N+:30]([O-:32])=[O:31]>>[CH3:15][C:16]1[C:21]([N+:22]([O-:24])=[O:23])=[C:20]([CH3:25])[C:19]([S:26]([CH2:29][CH2:1][CH3:2])(=[O:28])=[O:27])=[CH:18][C:17]=1[N+:30]([O-:32])=[O:31]

Participants

3

Reactant 2

HCID 14438868HCID 14438868, compoundHCID 22155650HCID 22155650, compound

Product 1

HCID 14438871HCID 14438871, compound

Procedure

2,4-Dimethyl-1-propylsulfonylbenzene (Beilstein H 5, page 491) was dinitrated analogously to (a).

Sources & evidence

ORD record
ord-5952910930b74c7a8bd707b7434ca153
Source dataset
uspto-grants-1990_12
Patent number
US04975516

Reaction notes

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