Potassium Carbonate → HCID 59032958, compound
Reaction equation
[OH:1][C:2]1[C:14]2[C:13](=[O:15])[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[C:6]=2[CH:5]=[CH:4][CH:3]=1.S(C1C=CC([N+]([O-])=O)=CC=1)(O[CH2:20][C@H:21]1[O:23][CH2:22]1)(=O)=O.C(=O)([O-])[O-].[K+].[K+]>>[O:23]1[CH2:22][C@H:21]1[CH2:20][O:1][C:2]1[C:14]2[C:13](=[O:15])[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[C:6]=2[CH:5]=[CH:4][CH:3]=1Participants
4
Procedure
Prepared from 1-hydroxy-9-fluorenone (3.0 g, 15.2 mmol), (S)-glycidyl nosylate (3.06 g, 15.2 mmol) and potassium carbonate (2.1 g, 15.2 mmol) according to the procedure used for Intermediate 1 to give 0.78 g product as a yellow solid.
Sources & evidence
- ORD record
- ord-a2ecfcb0dd1c4fc1a15344ac097e01ad
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06506901B2
Reaction notes
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