HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868404Generated: October 25, 2026
Indole → 1,1,1-trifluoro-3-(1H-indol-3-yl)propan-2-one oxime
https://huagongshe.com/reaction/1868404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Propanone,3-bromo-1,1,1-trifluoro-, oxime | HCID 2782273 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 1,1,1-trifluoro-3-(1H-indol-3-yl)propan-2-one oxime | HCID 76549379 | 89.2% |
Reaction Steps
To a solution of the 1.64 g (7.96 mmol) of 3-bromo-1,1,1-trifluoropropan-2-one oxime in 250 mL of methyl tert-butyl ether was added 3.74 g (31.92 mmol) of indole followed by 5.0 g (47.62 mmol) of powdered (freshly ground) sodium carbonate. The reaction was monitored by thin layer chromatography (ethyl acetate-hexanes (2:8)) to afford a new more polar product compared to indole (PMA-stained and UV-active). The mixture was then filtered through diatomaceous earth and concentrated in vacuo. The residue was then concentrated in vacuo and diluted first with dichloromethane (1 part) and then hexanes (4 parts) and passed through a pad of silica gel using dichloromethane-hexanes (gradient: 20%-100%) to afford 1.72 g (89.2%) of 1,1,1-trifluoro-3-(1H-indol-3-yl)propan-2-one oxime as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07635711B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-17a77fdf9e674e5b9d3fad3739dbfcc3 |
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| Source note | uspto-grants-2009_12 |
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