1,4-Dibromobutane → HCID 89751847, compound
Reaction equation
[OH:1][C:2]1[CH:7]=[C:6]([C:8](=[O:10])[CH3:9])[CH:5]=[CH:4][C:3]=1[C:11]1[CH:16]=[CH:15][C:14]([C:17](=[O:19])[CH3:18])=[CH:13][C:12]=1[OH:20].Br[CH2:22][CH2:23][CH2:24][CH2:25]Br>>[CH:4]1[C:3]2[C:11]3[CH:16]=[CH:15][C:14]([C:17](=[O:19])[CH3:18])=[CH:13][C:12]=3[O:20][CH2:25][CH2:24][CH2:23][CH2:22][O:1][C:2]=2[CH:7]=[C:6]([C:8](=[O:10])[CH3:9])[CH:5]=1Participants
3
Procedure
was synthesized from 1,1′-(2,2′-dihydroxy-[1,1′-biphenyl]-4,4′-diyl)-diethanone and 1,4-dibromobutane by following an analogous procedure described in Step 1, Example 1. m/z 325.2 (M+H)+.
Sources & evidence
- ORD record
- ord-29dc38c6f13c49abaf8908e4f29d51e6
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09073943B2
Reaction notes
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