Trimethyl borate → HCID 54083272, compound
Reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])=[CH:4][CH:3]=1.C([Li])CCC.[B:25](OC)([O:28]C)[O:26]C.C(OC1C=CC(B(O)O)=CC=1)CCCCCCC>C1COCC1>[CH2:9]([O:8][C:5]1[CH:6]=[CH:7][C:2]([B:25]([OH:28])[OH:26])=[CH:3][CH:4]=1)[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19]Participants
6
Procedure
Quantities: compound 29 (15.36 g, 0.047 mol) in anhydrous THF (200 ml), n-butyllithium (26 ml, 2.5M in hexane, 0.065 mol), trimethyl borate (9.79 g, 0.094 mol) in anhydrous THF (26 ml). The experimental procedure was as described for the preparation of compound 33.
Sources & evidence
- ORD record
- ord-8f72cfe2984543d1ae27c1e132e25be7
- Source dataset
- uspto-grants-1998_12
- Patent number
- US05853613
Reaction notes
Loading…