HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250562Generated: October 27, 2026
Water → N-(2,4-difluoro-3-formylphenyl)propane-2-sulfonamide
https://huagongshe.com/reaction/250562
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-(2,4-difluorophenyl)propane-2-sulfonamide | HCID 58087510 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2,4-difluoro-3-formylphenyl)propane-2-sulfonamide | HCID 58086031 | — |
Reaction Steps
To propane-2-sulfonic acid (2,4-difluoro-phenyl)-amide (59, 2.35 g, 9.95 mmol) in tetrahydrofuran (70 mL) under an atmosphere of nitrogen cooled with a dry ice/acetone bath was added 1.60 M of n-butyllithium (1.60 M in hexane, 6.53 mL, 10.45 mmol). The reaction was stirred for 40 minutes, and then another portion of n-butyllithium (1.60 M in hexane, 6.84 mL, 10.94 mmol). The reaction was stirred for 1 hour and N,N-dimethylformamide (0.92 mL, 11.9 mmol) was added. The reaction was allowed to warm to room temperature overnight. The reaction was poured into water extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and filtrated. The filtrate was concentrated and purified by silica gel column chromatography (dichloromethane/methanol 5%) to give the compound (60, 1.4 g, 53.4%). MS (ESI) [M−H+]−=263.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863288B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-031c3bf994ba4c64b75e558ff060b73c |
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| Source note | uspto-grants-2011_01 |
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