4-n-Octyloxyphenylboronic Acid (contains varying amounts of Anhydride) → HCID 19050464, compound
Reaction equation
Br[C:2]1[N:7]=[CH:6][C:5]([Br:8])=[CH:4][N:3]=1.[CH2:9]([O:17][C:18]1[CH:23]=[CH:22][C:21](B(O)O)=[CH:20][CH:19]=1)[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]>>[Br:8][C:5]1[CH:4]=[N:3][C:2]([C:21]2[CH:22]=[CH:23][C:18]([O:17][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])=[CH:19][CH:20]=2)=[N:7][CH:6]=1Participants
3
Procedure
2,5-Dibromopyrimidine and 4-octyloxybenzeneboronic acid are reacted analogously to Example 1 to give 5-bromo-2-(4-octyloxyphenyl) pyrimidine. ##STR34##
Sources & evidence
- ORD record
- ord-bfcdbbc2a21b462990d6f4474da4e9ae
- Source dataset
- uspto-grants-1995_09
- Patent number
- US05447656
Reaction notes
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