HCID 10728612, compound → HCID 12070572, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9](=[O:17])[CH:10]([CH3:16])[C:11]([O:13][CH2:14][CH3:15])=[O:12].C1OC2C(C3C4OCOC=4C=CC=3P(C3C=CC=CC=3)C3C=CC=CC=3)=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=CC=2O1>>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH:9]([OH:17])[CH:10]([CH3:16])[C:11]([O:13][CH2:14][CH3:15])=[O:12]Participants
3
Procedure
The thus obtained compound (5) is asymmetrically hydrogenated using ((R)—SEGPHOS™)-Ru complex to obtain optically active ethyl 4-(2-fluorophenyl)-3-hydroxy-2-methylbutyrate (6) as a mixture of diastereomers.
Sources & evidence
- ORD record
- ord-084af2cc9280444c8e18d6d8f3470fc4
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06717016B2
Reaction notes
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