1-(4-Iodophenyl)ethan-1-one → HCID 11390977, compound
Reaction equation
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][C:7]([I:10])=[CH:6][CH:5]=1)=[O:3].ClCC(OC(C1C=CC(I)=CC=1)C)=O>>[I:10][C:7]1[CH:8]=[CH:9][C:4]([C@@H:2]([OH:3])[CH3:1])=[CH:5][CH:6]=1Participants
3
Procedure
Starting from 4-iodophenyl methyl ketone, which is reduced to the racemic alcohol and converted to (±)-1-(4-iodophenyl)ethyl chloroacetate, the racemic ester is subjected to stereoselective enzyme hydrolysis. The remaining (S)-isomer of the ester is separated from the (R)-alcohol and transesterified to give (S)-1-(4-iodophenyl)ethanol (ee >98%) III.
Workup
- customThe remaining (S)-isomer of the ester is separated from the (R)-alcohol
Sources & evidence
- ORD record
- ord-fd8068368e3c41cd830ccacfce572f41
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07358369B2
Reaction notes
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