2-Propanone, 1-(3,4-dimethoxyphenyl)- → 3,4-Dma, (R)-
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][C:12](=O)[CH3:13])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].C1([C@H]([NH2:23])C)C=CC=CC=1>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][C@H:12]([NH2:23])[CH3:13])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]Participants
3
Procedure
Using 10 ml of the above cell-free extract, the mixture was reacted in a 100 ml reaction mixture comprising 0.1 M Tris-hydrochloric acid buffer (pH 8.5) containing 0.5 g 1-(3,4-dimethoxyphenyl)-2-propanone and 0.34 g (R)-1-phenylethylamine at 30° C. for 24 hours. As a result, 0.36 g (R)-(3,4-dimethoxyphenyl)-2-aminopropane was formed.
Workup
- extractionextract
- customthe mixture was reacted in a 100 ml reaction mixture comprising 0.1 M Tris-hydrochloric acid buffer (pH 8.5)
Sources & evidence
- ORD record
- ord-be10205f5ed941b3aea95d732fc2aaf4
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07169592B2
Reaction notes
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