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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantSodium CarbonateHCID 10340—
Reactant2-Propanone,3-bromo-1,1,1-trifluoro-, oximeHCID 2782273—
Solventtert-Butyl methyl etherHCID 15413—
Product1,1,1-trifluoro-3-(1H-indol-3-yl)propan-2-one oximeHCID 7654937989.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635711B2
Source datasetuspto-grants-2009_12
ORD IDord-17a77fdf9e674e5b9d3fad3739dbfcc3
Source noteuspto-grants-2009_12