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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844232Generated: October 29, 2026

Trifluoroacetic acid → HCID 15549971, compound

https://huagongshe.com/reaction/844232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantCyclohexanoneHCID 7967—
ReactantHCID 15549970HCID 15549970—
SolventAcetic AcidHCID 176—
ProductHCID 15549971HCID 1554997164%

Reaction Conditions

Temperature110 °C

Reaction Steps

In a 20 mL vial equipped with a screw cap and a stir bar was added cyclohexanone (0.1 mL; 0.88 mmol), trifluoroacetic acid (1 mL) and acetic acid (0.75 mL). The mixture was heated at 110° C. under argon for 15 minutes. A solution of compound (a), above, (0.07 g; 0.25 mmol) in acetic acid (1 mL) was added. The resulting mixture was stirred for an additional 20 minutes at 110° C. The reaction mixture was quenched with potassium hydroxide (1N) (pH: 10; 80 mL) and extracted with ethyl acetate (30 mL). The organic phase was successively washed with water (3×30 mL), brine (30 mL), dried (sodium sulfate), filtered and solvent was removed in vacuo. The residue was purified by column chromatography on silica gel using chloroform:methanol (95:5) to yield the title compound (0.6 g; 64%). 13C NMR (CDCl3): δ 148.6, 147.8, 138.0, 137.3, 134.5, 131.5, 130.9, 125.9, 123.5, 122.5, 121.8, 118.9, 118.4. 107.8, 45.8, 44.8, 34.2, 28.6, 25.8, 23.2, 22.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380242B1
Source datasetuspto-grants-2002_04
ORD IDord-7051f6104b1d4544a98591d0d8d2df1e
Source noteuspto-grants-2002_04