Phenacyl bromide → HCID 21319938, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[OH:9].Br[CH2:11][C:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=O>>[CH3:8][C:6]1[CH:7]=[C:2]([CH3:1])[C:3]2[O:9][CH:11]=[C:12]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[C:4]=2[CH:5]=1Participants
3
Procedure
Using the method of Example 17 and starting with 2,4-dimethylphenol and α-bromoacetophenone and cyclizing at 50°-60° C., 5,7-dimethyl-3-phenylbenzofuran is obtained.
Sources & evidence
- ORD record
- ord-66075a8250a442a79e625f5a5a5b916a
- Source dataset
- uspto-grants-1979_05
- Patent number
- US04153619
Reaction notes
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