11-Bromoundecanoic acid → Methyl 11-bromoundecanoate
Reaction equation
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]([OH:14])=[O:13].Br[CH2:16]CCCCC(O)=O>>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]([O:14][CH3:16])=[O:13]Participants
3
Procedure
12.0 grams (45 mmole) of 11-bromoundecanoic acid was treated in the same manner as described above for 6-bromohexanoic acid to yield greater than 90% methyl 11-bromoundecanoate.
Sources & evidence
- ORD record
- ord-4c98c9f3d36f4dfc80edf5b2ec14c299
- Source dataset
- uspto-grants-1992_03
- Patent number
- US05093471
Reaction notes
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