HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370611Generated: November 1, 2026
Trifluoroacetamide → HCID 178429266, compound
https://huagongshe.com/reaction/2370611
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetamide | HCID 67717 | — |
| Reactant | Magnesium monoxide | HCID 6850729 | — |
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Reactant | HCID 46947722 | HCID 46947722 | — |
| Catalyst | Rhodium acetate | HCID 168478 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178429266 | HCID 178429266 | 34% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710091B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-53ba4ac874494085a198bb939f594932 |
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| Source note | uspto-grants-2014_04 |
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