2-Fluoroethyl bromide → HCID 85990906, compound
Reaction equation
[NH2:1][CH2:2][CH:3]([O:7][CH2:8][CH3:9])[O:4][CH2:5][CH3:6].Br[CH2:11][CH2:12][F:13].C(N(C(C)C)CC)(C)C>CCOCC>[CH2:5]([O:4][CH:3]([O:7][CH2:8][CH3:9])[CH2:2][NH:1][CH2:11][CH2:12][F:13])[CH3:6]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 3.1 ml (21.5 mmol) of 1-amino-2,2-diethoxyethane, 3.0 g (23.6 mmol) of 1-bromo-2-fluoroethane and 5.56 g (43 mmol) of diisopropylethylamine was heated at 100° C. in a closed vessel for 6 hours. The reaction mixture was diluted with ether and washed with 1N NaOH and water. The organic phase was dried (MgSO4) and concentrated in vacuo. The residue was distilled in vacuo. 1.3 g of substance were obtained as a clear liquid.
Workup
- washwashed with 1N NaOH and water
- dry with materialThe organic phase was dried (MgSO4)
- concentrationconcentrated in vacuo
- distillationThe residue was distilled in vacuo
- custom1.3 g of substance were obtained as a clear liquid
Sources & evidence
- ORD record
- ord-9d77c5e7d7f1457881bb69c4f2333c33
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07652007B2
Reaction notes
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