HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973188Generated: October 31, 2026
Methanesulfonamide → N-methanesulfonyl (3-trifluoromethylphenoxy)(4-chlorophenyl)acetamide
https://huagongshe.com/reaction/973188
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-Chloro-α-[3-(trifluoromethyl)phenoxy]benzeneacetyl chloride | HCID 12109235 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-methanesulfonyl (3-trifluoromethylphenoxy)(4-chlorophenyl)acetamide | HCID 54399462 | — |
Reaction Steps
(3-Trifluoromethylphenoxy)(4-chlorophenyl)acetyl chloride (0.02 mole) in tetrahydrofuran (50 ml.) is added over a 15-minute period to a solution of the sodium salt of methanesulfonamide (2.5 g., 0.021 mole) in tetrahydrofuran (50 ml.) at 0°-5° C., under a nitrogen atmosphere. The mixture is stirred at 20° C. for 20 hours and then the solvent is evaporated under vacuum. The residue is dissolved in chloroform and the solution is extracted with water. The chloroform solution is dried over anhydrous magnesium sulfate, filtered and the solvent removed to afford N-methanesulfonyl (3-trifluoromethylphenoxy)(4-chlorophenyl)acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04055592 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-0bd7c8a44bae46cbb1d40663e8710c2c |
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| Source note | uspto-grants-1977_10 |
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