3-Hydroxybenzaldehyde → 3-Propoxybenzaldehyde
Reaction equation
[CH2:1]([O:4][C:5]1[CH:6]=[C:7](/[CH:11]=C/C(Cl)=O)[CH:8]=[CH:9][CH:10]=1)[CH2:2][CH3:3].[OH:16]C1C=C(C=CC=1)C=O.ICCC>>[CH2:1]([O:4][C:5]1[CH:6]=[C:7]([CH:8]=[CH:9][CH:10]=1)[CH:11]=[O:16])[CH2:2][CH3:3]Participants
4
Procedure
For example, (E)-3-(3′-propyloxyphenyl)-2-propenoyl chloride, used in Example 3 (i), can be prepared from commercially available 3-hydroxybenzaldehyde by reacting 3-hydroxybenzaldehyde with 1-iodopropane to give 3-propyloxy benzaldehyde. 3-Propyloxy benzaldehyde is then reacted with malonic acid to give the corresponding propenonic acid which is subsequently converted into (E)-3-(3′-propyloxyphenyl)-2-propenoyl chloride by reaction with oxalyl chloride.
Sources & evidence
- ORD record
- ord-4c2a0d5443ee404f8f41376cbfacdc46
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06441173B1
Reaction notes
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