Methyl iodide → HCID 57905276, compound
Reaction equation
[F:1][CH2:2][CH2:3][NH:4][C:5](=[O:11])[O:6][C:7]([CH3:10])([CH3:9])[CH3:8].[H-].[Na+].I[CH3:15]>C1COCC1>[F:1][CH2:2][CH2:3][N:4]([CH3:15])[C:5](=[O:11])[O:6][C:7]([CH3:8])([CH3:10])[CH3:9]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of tert-butyl 2-fluoroethylcarbamate (4.1 g, 25.1 mmol) in THF (100 mL) at 0° C. was added sodium hydride, 60 wt % in mineral oil (1.507 g, 37.7 mmol) portion-wise. The reaction was stirred under N2 for 15 minutes after which gas evolution ceased. Iodomethane (2.356 mL, 37.7 mmol) was added drop-wise and the reaction stirred under N2. After 6 h, the reaction was quenched with water (100 mL) and concentrated. The aqueous solution was washed with CH2Cl2 (3×50 mL). The CH2Cl2 extracts were combined, washed with water (2×100 mL), dried (MgSO4) and concentrated to afford the title compound (4.0 g, 90% yield) as a clear oil. 1H NMR (400 MHz, CDCl3) δ: 4.58 (1H, brs), 4.47 (1 H, brs), 3.53 (1 H, brs), 3.47 (1 H, brs), 2.94 (3 H, s), 1.45 (9 H, s).
Workup
- stirringthe reaction stirred under N2
- waitAfter 6 h
- customthe reaction was quenched with water (100 mL)
- concentrationconcentrated
- washThe aqueous solution was washed with CH2Cl2 (3×50 mL)
- washwashed with water (2×100 mL)
- dry with materialdried (MgSO4)
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-588e767e80bc4210ab988e5671547c2b
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08129398B2
Reaction notes
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