Methyl iodide → HCID 11074136, compound
Reaction equation
O1CCC[CH2:2]1.[Si]([O:13][C:14]([NH:16][CH:17]([CH2:22][CH:23]=[CH2:24])[C:18]([O:20][CH3:21])=[O:19])=[O:15])(C(C)(C)C)(C)C.CI.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O>[CH3:2][O:13][C:14]([NH:16][CH:17]([CH2:22][CH:23]=[CH2:24])[C:18]([O:20][CH3:21])=[O:19])=[O:15]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
To a tetrahydrofuran solution (3.0 ml) of the compound prepared in Example 3 (170 mg, 0.59 mmol), were successively added dropwise at 0° C. in a nitrogen atmosphere methyl iodide (0.074 ml, 1.18 mmol) and a tetrahydrofuran solution of tetrabutylammonium fluoride (0.59 ml, 0.59 mmol). The mixture was agitated for 1 hour at 0° C., poured into water and extracted with ether. The ether layer was dried over anhydrous magnesium sulfate and the solvent was distilled off under vacuum. The resulting reaction mixture was subjected to column chromatography and eluted with a 1:4 mixture of ether and hexane to give 93 mg of the titled compound (yield, 84% based on the starting materials used in Example 3).
Workup
- extractionextracted with ether
- dry with materialThe ether layer was dried over anhydrous magnesium sulfate
- distillationthe solvent was distilled off under vacuum
- customThe resulting reaction mixture
- washeluted with a 1:4 mixture of ether and hexane
Sources & evidence
- ORD record
- ord-7a2608409c214c978094489ca36fa32c
- Source dataset
- uspto-grants-1989_06
- Patent number
- US04837349
Reaction notes
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