4-Bromobenzaldehyde → (R)-1-(4-bromobenzyl)-3-fluoropyrrolidine
Reaction equation
Cl.[F:2][C@@H:3]1[CH2:7][CH2:6][NH:5][CH2:4]1.[Br:8][C:9]1[CH:16]=[CH:15][C:12]([CH:13]=O)=[CH:11][CH:10]=1>>[Br:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13][N:5]2[CH2:6][CH2:7][C@@H:3]([F:2])[CH2:4]2)=[CH:11][CH:10]=1Participants
3
Procedure
The title compound was synthesized according to the method of Example A105B, except substituting (R)-3-fluoropyrrolidine hydrochloride (576 mg, 4.59 mmol) and 4-bromobenzaldehyde (849 mg, 4.59 mmol) which gave 1.09 g, 91% of a clear, colourless oil; MS ESI [M+H]+ 258.0, calcd for [C11H13BrFN+H]+ 258.03.
Workup
- customgave 1.09 g, 91% of a clear, colourless oil
Sources & evidence
- ORD record
- ord-3741c2583aad4bce8c2be260e15c1b56
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08481533B2
Reaction notes
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