Acetic acid, 2,2'-[methylenebis(sulfonyl)]bis- → 4-((1E)-2-(((E)-2-Fluoro-4-cyanostyrylsulfonyl)methylsulfonyl)vinyl)-3-fluorobenzonitrile
Reaction equation
[F:1][C:2]1[CH:9]=[C:8]([C:10]#[N:11])[CH:7]=[CH:6][C:3]=1[CH:4]=O.C([CH2:15][S:16]([CH2:19][S:20]([CH2:23][C:24](O)=O)(=[O:22])=[O:21])(=[O:18])=[O:17])(O)=O>C(O)(=O)C>[F:1][C:2]1[CH:9]=[C:8]([C:10]#[N:11])[CH:7]=[CH:6][C:3]=1/[CH:4]=[CH:15]/[S:16]([CH2:19][S:20](/[CH:23]=[CH:24]/[C:3]1[CH:6]=[CH:7][C:8]([C:10]#[N:11])=[CH:9][C:2]=1[F:1])(=[O:22])=[O:21])(=[O:18])=[O:17]Participants
4
Procedure
A solution of 2-fluoro-4-cyanobenzaldehyde (2 mmol) and carboxymethane-sulfonylmethanesulfonyl-acetic acid (1 mmol) in acetic acid (10 mL) was subjected to General Procedure 1, to yield the title compound in 72% yield. m.p. 268-270° C.
Sources & evidence
- ORD record
- ord-65654a6e964b42d595b6e724f3f8606e
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08058313B2
Reaction notes
Loading…