Benzoic acid, 3-formyl-4-hydroxy-, methyl ester → Methyl 3-formyl-4-(trifluoromethylsulfonyloxy)benzoate
Reaction equation
[CH:1]([C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:12]=1[OH:13])[C:6]([O:8][CH3:9])=[O:7])=[O:2].CC1(C)C(C2C=C(C=CC=2[O:30][S:31]([C:34]([F:37])([F:36])[F:35])(=O)=[O:32])C(OC)=O)=CCC1>>[CH:1]([C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:12]=1[O:13][S:31]([C:34]([F:37])([F:36])[F:35])(=[O:32])=[O:30])[C:6]([O:8][CH3:9])=[O:7])=[O:2]Participants
3
Procedure
Compound 66.41B was synthesized from methyl 3-formyl-4-hydroxybenzoate 66.41A (commercially available from Aldrich) using a method analogous to the method used to prepare compound 66.6I from 66.6H. MS ESI m/e: 313.2 (M+H)+.
Sources & evidence
- ORD record
- ord-02dc27b049ff4922bf9eab85b95c371b
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030354B2
Reaction notes
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