1-Bromo-3-methoxypropane → 1-[3-Tert-butyl-4-methoxy-5-(3-methoxypropoxy)phenyl]ethanone
Reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([C:14](=[O:16])[CH3:15])[CH:8]=[C:9]([OH:13])[C:10]=1[O:11][CH3:12])([CH3:4])([CH3:3])[CH3:2].Br[CH2:18][CH2:19][CH2:20][O:21][CH3:22]>>[C:1]([C:5]1[CH:6]=[C:7]([C:14](=[O:16])[CH3:15])[CH:8]=[C:9]([O:13][CH2:18][CH2:19][CH2:20][O:21][CH3:22])[C:10]=1[O:11][CH3:12])([CH3:4])([CH3:2])[CH3:3]Participants
3
Procedure
1-(3-tert-Butyl-5-hydroxy-4-methoxyphenyl)ethanone (O3.070; 2.00 g) and 1-bromo-3-methoxypropane (1.65 g) were converted, worked up and purified analogously to O2.110. 1.50 g of the title compound were obtained.
Workup
- custompurified analogously to O2
Sources & evidence
- ORD record
- ord-cb5017dc1e7140219b08dd73446aecb9
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08076336B2
Reaction notes
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