Pyrrolidine → (Tetrahydro-3,3-diphenyl-2-furylidene)pyrrolidinium bromide
Reaction equation
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[Br-:6].C[N+](C)=[C:9]1[C:13]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:12][CH2:11][O:10]1>>[Br-:6].[C:14]1([C:13]2([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:12][CH2:11][O:10][C:9]2=[N+:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1Participants
3
Procedure
Compound (G) 1-(3,3-diphenyl-dihydrofuran-2-ylidene)-pyrrolidinium bromide was prepared with pyrrolidine following the same procedure as the synthesis of compound (F) dimethyl(tetrahydro-3,3-diphenyl-2-furylidene)ammonium bromide.
Sources & evidence
- ORD record
- ord-f856fb45ade54ec0babd01809c0b8d08
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08481743B2
Reaction notes
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