Isopropyl iodide → 2-Methyl-4-[(propan-2-yl)oxy]benzaldehyde
Reaction equation
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[C:4]([CH3:10])[CH:3]=1.I[CH:12]([CH3:14])[CH3:13]>>[CH3:10][C:4]1[CH:3]=[C:2]([O:1][CH:12]([CH3:14])[CH3:13])[CH:9]=[CH:8][C:5]=1[CH:6]=[O:7]Participants
3
Procedure
The compound was synthesized as in Example 87.1, using 4-hydroxy-2-methylbenzaldehyde (54.4 mg, 0.40 mmol) in place of 4-hydroxybenzaldehyde and 2-iodopropane (100 μL, 0.80 mmol) in place of 1-iodo-(3,3,3-trifluoro)propane to give 2-methyl-4-isopropoxybenzaldehyde (54 mg, 76%). Used without further characterization.
Workup
- customThe compound was synthesized as in Example 87.1
Sources & evidence
- ORD record
- ord-a5a6120f75b04621a2d6eaa3f1d42723
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09315495B2
Reaction notes
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