Potassium Carbonate → HCID 60078038, compound
Reaction equation
[CH2:1]([S:3]([C:6]1[O:10][C:9]2[CH:11]=[CH:12][CH:13]=[C:14]([OH:15])[C:8]=2[CH:7]=1)(=[O:5])=[O:4])[CH3:2].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+]>>[CH2:1]([S:3]([C:6]1[O:10][C:9]2[CH:11]=[CH:12][CH:13]=[C:14]([O:15][CH2:20][C@H:21]3[O:23][CH2:22]3)[C:8]=2[CH:7]=1)(=[O:4])=[O:5])[CH3:2]Participants
4
Procedure
By the reactions in the same manner as in Starting Material Synthesis Example 1 using 2-(ethylsulfonyl)-4-hydroxybenzo(b)furan (2.75 g), (S)-glycidyl nosylate (3.48 g) and potassium carbonate (5.05 g), a crude product of the title compound (3.62 g) was obtained as a pale-yellow oil.
Sources & evidence
- ORD record
- ord-307af693f7d142f19c5f8d125f386983
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06720320B2
Reaction notes
Loading…