1-Bromo-2-methylpropane → HCID 69310804, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:7]([C:12]2[C:13]([C:18]3[CH:23]=[C:22]([Cl:24])[CH:21]=[CH:20][C:19]=3[OH:25])=[CH:14][CH:15]=[CH:16][CH:17]=2)=[CH:8][CH:9]=[CH:10][CH:11]=1)=[O:5])[CH3:2].Br[CH2:27][CH:28]([CH3:30])[CH3:29]>>[CH2:1]([O:3][C:4]([C:6]1[C:7]([C:12]2[C:13]([C:18]3[CH:23]=[C:22]([Cl:24])[CH:21]=[CH:20][C:19]=3[O:25][CH2:27][CH:28]([CH3:30])[CH3:29])=[CH:14][CH:15]=[CH:16][CH:17]=2)=[CH:8][CH:9]=[CH:10][CH:11]=1)=[O:5])[CH3:2]Participants
3
Procedure
Prepared as in procedure A from 5-chloro-2-hydroxy-[1,1′;2′,1″]terphenyl-2″-carboxylic acid ethyl ester and 1-bromo-2-methyl-propane.
Sources & evidence
- ORD record
- ord-c8ea42d0ffc14b9ea20d0696f3e46746
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07446222B2
Reaction notes
Loading…