Diazomethane → HCID 53969069, compound
Reaction equation
[F:1][C:2]([F:10])([F:9])[C@:3]([OH:8])([CH3:7])[C:4]([OH:6])=[O:5].[N+](=[CH2:13])=[N-]>CCOCC>[F:1][C:2]([F:10])([F:9])[C@:3]([OH:8])([CH3:7])[C:4]([O:6][CH3:13])=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (S)-3,3,3-trifluoro-2-hydroxy-2-methylpropionic acid (3.0 g, 17.4 mmol) in 60 ml of ether was added a solution of diazomethane in ether until a yellow coloration remained. The reaction mixture was then stirred 30 min at room temperature and concentrated to dryness to afford the title compound. 1H NMR (400 MHz, acetone-d6): δ 5.67 (s, 1H), 3.85 (s, 3H), 1.57 (s, 3H).
Workup
- concentrationconcentrated to dryness
Sources & evidence
- ORD record
- ord-432e92ed0e994064af957311574dc2ae
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07553973B2
Reaction notes
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