HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042943Generated: October 25, 2026
Trifluoroacetamide → dimethyl 2,2'[N-(trifluoroacetyl)sulfonimidoyl]diacetate
https://huagongshe.com/reaction/1042943
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetamide | HCID 67717 | — |
| Reactant | Magnesium monoxide | HCID 6850729 | — |
| Reactant | Thionyldiacetic acid dimethylester | HCID 10997883 | — |
| Reactant | Bis(acetoxy)iodobenzene | HCID 21865429 | — |
| Catalyst | Dirhodium tetraacetate | HCID 152122 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | dimethyl 2,2'[N-(trifluoroacetyl)sulfonimidoyl]diacetate | HCID 86668547 | 98.4% |
Reaction Steps
Trifluoroacetamide (5.43 g, 2 eq), magnesium oxide (3.756 g, 4 eq), and rhodium(II) acetate dimer (309 mg, 0.03 eq) were placed in a 500 mL round-bottom flask. Dichloromethane (230 mL) was added followed by dimethyl 2,2′-sulfinyldiacetate (4.52 g, 23.3 mmol, 1 eq), followed by addition of diacetoxyiodobenzene in small portions (11.257 g, 1.5 eq). The mixture was stirred at room temperature for 7 hours. Following that, an additional 2.2 g of trifluoroacetamide was added followed by the addition of additional amount of rhodium(II) acetate dimer (˜150 mg) and diacetoxyiodobenzene (3.0 g). The reaction mixture was stirred further at room temperature overnight. The mixture was then filtered through a pad of celite and the pad was washed with MeOH—CHCl3 (1:5). The filtrate was concentrated and the oily residue was subject to column chromatography twice (from hexane to EtOAc-Hex 1:1) yielding dimethyl 2,2′-[N-(trifluoroacetyl)sulfonimidoyl]diacetate as a brown oil (7.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08558002B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-71be56af3dd44a28968c6b98b1063407 |
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| Source note | uspto-grants-2013_10 |
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