Nonanoyl chloride → 4-(S)-Isopropyl-3-(1-oxononyl)-2-oxazolidinone
Reaction equation
[CH:1]([C@H:4]1[CH2:8][O:7][C:6](=[O:9])[NH:5]1)([CH3:3])[CH3:2].[C:10](Cl)(=[O:19])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]>>[CH:1]([C@H:4]1[CH2:8][O:7][C:6](=[O:9])[N:5]1[C:10](=[O:19])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])([CH3:3])[CH3:2]Participants
3
Procedure
Following the procedure described in Referential Example 3, but using 4-(S)-isopropyl-2-oxazolidinone (4.99 g) and nonanoyl chloride (7.16 g), the desired compound (10.12 g) was obtained.
Sources & evidence
- ORD record
- ord-ca72507f5c1b4a7d9f6f2c580aada948
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05643908
Reaction notes
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