Dichloromethane → 6-Fluoro-3-methyl-5-nitro-1,2-benzisothiazole
Reaction equation
Cl[C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]2[C:6]([CH3:9])=[N:7][S:8][C:4]=2[CH:3]=1.[F-:15].[K+].C1OCCOCCOCCOCCOCCOC1.C(Cl)Cl>C(#N)C.C(OCC)(=O)C>[F:15][C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]2[C:6]([CH3:9])=[N:7][S:8][C:4]=2[CH:3]=1Participants
Procedure
A mixture of 6-chloro-3-methyl-5-nitro-1,2-benzisothiazole (2.25 g, 9.80 mmol), potassium fluoride (2.85 g, 49.0 mmol), and 18-crown-6 (1.50 g, 5.70 mmol) in acetonitrile is heated in a sealed tube for 29 days, filtered to remove solids, and partially concentrated in vacuo to obtain a liquid. The liquid is diluted with ethyl acetate, washed sequentially with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a dark, brown solid. Flash column chromatography of the solid using silica gel and a 10% to 50% ethyl acetate in hexanes gradient gives a yellow solid containing two components. Flash column chromatography of the yellow solid using silica gel and a 50% to 70% methylene chloride in hexanes gradient gives the title product as a pale, yellow solid (0.870 g, mp 118-119° C.) which is identified by NMR spectral analyses.
Workup
- temperatureis heated in a sealed tube for 29 days
- filtrationfiltered
- customto remove solids
- concentrationpartially concentrated in vacuo
- customto obtain a liquid
- washwashed sequentially with water and brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated in vacuo
- customto obtain a dark, brown solid
- additioncontaining two components
Sources & evidence
- ORD record
- ord-2b007e66851b4d209ac20a77513a4095
- Source dataset
- uspto-grants-2000_10
- Patent number
- US06140270
Reaction notes
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