Methyl fluorosulfate → HCID 86737691, compound
Reaction equation
[CH2:1]([O:5][C:6]1[CH:10]=[CH:9][S:8][N:7]=1)[CH2:2][CH2:3][CH3:4].[F:11][S:12]([O:15][CH3:16])(=[O:14])=[O:13]>>[F:11][S:12]([O-:15])(=[O:14])=[O:13].[CH2:1]([O:5][C:6]1[CH:10]=[CH:9][S:8][N+:7]=1[CH3:16])[CH2:2][CH2:3][CH3:4]Participants
3
Procedure
3-n-Butoxyisothiazole (7.2 g, 0.046 mol) and 8 ml of methyl fluorosulfonate were heated to 70° for 1 hr. After cooling, the solid was washed with ether and dried to yield 8.7 g of 3-n-butoxy-2-methylisothiazolium fluorosulfonate a low melting solid. Spectral data (NMR & IR) were consistent with the assigned structure.
Workup
- temperatureAfter cooling
- washthe solid was washed with ether
- customdried
Sources & evidence
- ORD record
- ord-4004dc9bc35446909e00d38e7e71e638
- Source dataset
- uspto-grants-1981_04
- Patent number
- US04262127
Reaction notes
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