HCID 178460834, compound → HCID 178477622, compound

HRID 1579222Notes

Reaction equation

HRID 1579222 reaction equation
C(SCC1C=[N+]([O-])C2C(=CC=CC=2)[N+]=1[O-])CC.[CH2:18]([S:21]([CH2:23][C:24]1[CH:33]=[N+:32]([O-:34])[C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[N+:25]=1[O-:35])=[O:22])[CH2:19]C>>[CH2:18]([S:21]([CH2:23][C:24]1[CH:33]=[N+:32]([O-:34])[C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[N+:25]=1[O-:35])=[O:22])[CH3:19]

Participants

3

Reactant 2

HCID 178460834HCID 178460834, compoundHCID 178461003HCID 178461003, compound

Product 1

HCID 178477622HCID 178477622, compound

Procedure

By means of this procedure, 2-n-propylthiomethylquinoxaline 1,4-dioxide is converted in 73 percent yield to 2-n-propylsulfinylmethylquinoxaline 1,4-dioxide, m.p. 137°-139°C.

Sources & evidence

ORD record
ord-0f9cef2a542346378136e63795e46f17
Source dataset
uspto-grants-1976_01
Patent number
US03931174

Reaction notes

Loading…