HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449621Generated: October 30, 2026
Sodium Trifluoroacetate → HCID 11745639, compound
https://huagongshe.com/reaction/1449621
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Trifluoroacetate | HCID 517019 | — |
| Reactant | 1H-Indole, 2-iodo-1-methyl- | HCID 11065059 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 11745639 | HCID 11745639 | 37% |
Reaction Steps
A mixture of 1-methyl-2-iodoindole (4.40 g, 17.3 mmole), sodium trifluoroacetate (24.0 g, 176.5 mmole) and copper(I) iodide (17.1 g, 89.8 mmole) in N-methylpyrrolidone is heated at 160° C. for 6 hours, cooled to room temperature, diluted with water and filtered through diatomaceous earth to remove copper salts. The filtrate is extracted with ether. The extracts are combined, washed with water, dried over MgSO4 and concentrated in vacuo to give a residue. The residue is chromatographed using silica gel and 4:1 hexanes:ethyl acetate as eluent to give the title product as a pale yellow oil which crystallized on standing, 119 g (37% yield), mp 28°-32° C., identified by IR, 1HNMR and 19FNMR analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05599832 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-2663fa617e9048648adb15c309d5b1e1 |
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| Source note | uspto-grants-1997_02 |
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