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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370611Generated: November 1, 2026

Trifluoroacetamide → HCID 178429266, compound

https://huagongshe.com/reaction/2370611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetamideHCID 67717—
ReactantMagnesium monoxideHCID 6850729—
ReactantIodo benzene diacetateHCID 12217721—
ReactantHCID 46947722HCID 46947722—
CatalystRhodium acetateHCID 168478—
SolventDichloromethaneHCID 6344—
ProductHCID 178429266HCID 17842926634%

Reaction Conditions

Temperature23 °C

Reaction Steps

2,2,2-trifluoroacetamide (106 mg, 0.94 mmole), magnesium oxide (76 mg, 4 eq.), rhodium acetate in the dimer form (5.2 mg, 0.025 eq.) and iodobenzene diacetate (228 mg, 1.5 eq.) are added at 23° C. to a solution of Example 1 (300 mg, 0.48 mmole) in anhydrous CH2Cl2 (5 ml). Stirring is maintained for 6 hours at 23° C. then the reaction mixture is filtered under vacuum. The filtrate is poured into water (25 ml) and extracted with AcOEt (2×25 ml). The organic phases are combined and washed successively with water (25 ml) and salt water (25 ml). After drying over Na2SO4, the organic solution is filtered and concentrated under vacuum. The evaporation residue is purified on a silica column (eluent: Heptane/AcOEt:5/5 to 3/7). After collection and concentration of the pure fractions, the expected compound is obtained in the form of a colourless oil with a yield of 34% (77 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710091B2
Source datasetuspto-grants-2014_04
ORD IDord-53ba4ac874494085a198bb939f594932
Source noteuspto-grants-2014_04