Methyl iodide → 6-Methoxy-2-methylbenzo[b]thiophene
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[CH:10]=[CH:9][S:8][C:7]=2[CH:11]=1.[CH3:12]I>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[CH:10]=[C:9]([CH3:12])[S:8][C:7]=2[CH:11]=1Participants
3
Procedure
The same operations as in Preparation example 1 were carried out using 180 mg of 6-methoxybenzo[b]thiophene, and 450 mg of methyl iodide in place of cyclohexanone, and then purification was carried out by TLC (developing solvent, chloroform:n-hexane=1:19) to obtain 126 mg of 6-methoxy-2-methylbenzo[b]thiophene.
Workup
- customThe same operations as in Preparation example 1
- custompurification
Sources & evidence
- ORD record
- ord-c6041b427f3842f89710d39091a12f47
- Source dataset
- uspto-grants-1995_12
- Patent number
- US05472962
Reaction notes
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