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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862505Generated: November 4, 2026

Trifluoroacetic acid → HCID 86757494, compound

https://huagongshe.com/reaction/1862505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAmmonium HydroxideHCID 14923—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 22982929HCID 22982929—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86757494HCID 8675749448%

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Choroacetyl-N-trifluoroacetyl-(R)-1-aminoindan (30.57 g, 0.1 mol) was dissolved in anhydrous dichloromethane (210 ml) and 3-chloroperoxybenzoic acid (70%, 44.87 g, 0.26 mol) was added all at once. The suspension was cooled to 0° C. and trifluoroacetic acid (11.4 g, 0.1 mol) was added dropwise for 5-10 minutes. The reaction flask was protected from light and the mixture was stirred for 3-5 days at room temperature. The reaction mixture was poured into water (300 ml.). The mixture was neutralized with ammonium hydroxide solution. The layers were separated. The aqueous layer was extracted with dichloromethane (200 ml). The combined organic layers were dried (Na2SO4) and the solvent was removed under reduced pressure to give a solid, which was recrystallized from ethanol to give 15 g (48%) of a white solid mp: 169-170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06538025B2
Source datasetuspto-grants-2003_03
ORD IDord-d4da5fac34194aec8128b6a54ab6bb93
Source noteuspto-grants-2003_03