4,5-Dimethyl-1,2-phenylenediamine → HCID 178422342, compound
Reaction equation
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([NH2:9])=[C:4]([NH2:10])[CH:3]=1.C(O[C:14]([S-])=[S:15])C.[K+]>>[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]2[N:9]=[C:14]([SH:15])[NH:10][C:4]=2[CH:3]=1Participants
3
Procedure
Reaction of 30 g (0.22 mole) of 4,5-dimethyl-1,2-phenylenediamine with potassium ethylxanthate using the method described in Example 86 yielded 19 g of 5,6-dimethyl-2-mercaptobenzimidazole, as confirmed by the nmr and infrared spectra and by elemental analysis. The title compound (3.0 g) was prepared by the method of Example 84 using 3.5 g of 5,6-dimethyl-2-mercaptobenzimidazole instead of 2-mercaptobenzimidazole. Structure assignment was supported by the nmr spectrum.
Sources & evidence
- ORD record
- ord-6fc87bf052be403597a2584179f0d105
- Source dataset
- uspto-grants-2005_06
- Patent number
- US06906078B2
Reaction notes
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