Dicyclohexylcarbodiimide → 428452-46-4
Reaction equation
[F:1][C:2]([F:10])([CH2:6][C:7]([OH:9])=[O:8])[C:3]([OH:5])=[O:4].[CH:11]1(N=C=NC2CCCCC2)CCCCC1>C1COCC1>[CH3:11][O:4][C:3](=[O:5])[C:2]([F:10])([F:1])[CH2:6][C:7]([OH:9])=[O:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Commercially available 2,2-difluorosuccinic acid (8.0 g, 51.9 mmol) was dissolved in THF and cooled on ice before addition of 1,3-dicyclohexylcarbodiimide (11.8 g, 57.2 mmol). The mixture was stirred at room temperature for 3 hours, cooled and filtered. The filtrate was concentrated in vacuo. The residue was stirred with methanol (50 ml) for 3 hours at room temperature and then solvents were removed in vacuo to afford the crude ester as an oil (8.4 g). The oil was purified by column chromatography on silica gel column and elution with a 0-100% ethyl acetate/toluene gradient to afford 2,2-difluorosuccinic acid 1-methyl ester as a colorless oil (6.8 g).
Workup
- temperaturecooled
- filtrationfiltered
- concentrationThe filtrate was concentrated in vacuo
- stirringThe residue was stirred with methanol (50 ml) for 3 hours at room temperature
- customsolvents were removed in vacuo
- customto afford the crude ester as an oil (8.4 g)
- customThe oil was purified by column chromatography on silica gel column and elution with a 0-100% ethyl acetate/toluene gradient
Sources & evidence
- ORD record
- ord-cd6f12bc4f3f45308e5b34d9da9ad1b1
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06821960B2
Reaction notes
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