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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetamideHCID 67717—
ReactantMagnesium monoxideHCID 6850729—
ReactantThionyldiacetic acid dimethylesterHCID 10997883—
ReactantBis(acetoxy)iodobenzeneHCID 21865429—
CatalystDirhodium tetraacetateHCID 152122—
SolventDichloromethaneHCID 6344—
Productdimethyl 2,2'[N-(trifluoroacetyl)sulfonimidoyl]diacetateHCID 8666854798.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08558002B2
Source datasetuspto-grants-2013_10
ORD IDord-71be56af3dd44a28968c6b98b1063407
Source noteuspto-grants-2013_10