Methanesulfonic Acid → Methane
Reaction equation
[C:1]1([CH3:10])[CH:6]=[CH:5][C:4](S([O-])=O)=[CH:3][CH:2]=1.[Na+].[CH2:12]([N:14]([CH2:24]C)[C:15]1[CH:20]=[CH:19][CH:18]=[C:17](OCC)[CH:16]=1)C.[CH3:26][S:27]([OH:30])(=O)=[O:28]>>[CH4:1].[CH3:24][N:14]([CH3:12])[C:15]1[CH:16]=[CH:17][C:18]([C:2]2[C:3]([C:18]3[CH:19]=[CH:20][C:15]([N:14]([CH3:24])[CH3:12])=[CH:16][CH:17]=3)=[C:4]([S:27]([CH3:26])(=[O:30])=[O:28])[CH:5]=[CH:6][C:1]=2[CH3:10])=[CH:19][CH:20]=1Participants
5
Procedure
Ten and three tenths grams of 86.4 percent sodium p-toluenesulfinate, 10.7 g of 90.7 percent N,N-diethyl-3-ethoxyaniline and 12 g of 4-(N-ethyl-N-benzyl)-aminobenzaldehyde were interacted in the presence of 18.2 g of 95 percent methanesulfonic acid to obtain a methane of Formula XV wherein R=4--CH3 ; R5 =C2H5O; R6 =N(C2H5)2 ; Q=4--[(C2H5)(C6H5CH2)NC6H4 ], an oil. A significant infrared maximum appeared at 1145 (SO2 ; s) cm-1. The product developed a violet colored image.
Sources & evidence
- ORD record
- ord-1d4c91b81707442fa2df58279e46075d
- Source dataset
- uspto-grants-1981_03
- Patent number
- US04257954
Reaction notes
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