Formic Acid → HCID 19738514, compound
Reaction equation
[F:1][CH2:2][C:3](=[CH2:17])[CH2:4][N:5]([CH2:11][CH:12](OC)[O:13]C)[C:6](=[O:10])[O:7][CH2:8][CH3:9].C(O)=O.[Cl-].[Na+]>O>[F:1][CH2:2][C:3](=[CH2:17])[CH2:4][N:5]([CH2:11][CH:12]=[O:13])[C:6](=[O:10])[O:7][CH2:8][CH3:9]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
25 g (0.1 mol) of ethyl N-(2-fluoromethylallyl)-N-(2,2-dimethoxyethyl)carbamate are heated under reflux for two hours with 5 g of formic acid in 100 ml of water. The mixture is saturated with sodium chloride and extracted with methylene chloride, and the organic phases are washed with sodium hydrogen carbonate solution until neutral. They are dried over magnesium sulphate and concentrated, and the residue is distilled.
Workup
- extractionextracted with methylene chloride
- washthe organic phases are washed with sodium hydrogen carbonate solution until neutral
- dry with materialThey are dried over magnesium sulphate
- concentrationconcentrated
- distillationthe residue is distilled
Sources & evidence
- ORD record
- ord-6c9d753a72fb40c2bd484b8a7a4d4173
- Source dataset
- uspto-grants-1993_08
- Patent number
- US05241076
Reaction notes
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