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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043324Generated: November 2, 2026

Acetone → HCID 21043795, compound

https://huagongshe.com/reaction/2043324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant4-Chloro-3-(trifluoromethyl)anilineHCID 67574—
ReactantSodium cyanoborohydrideHCID 5003444—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
ProductHCID 21043795HCID 2104379574.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

5-Amino-2-chlorobenzotrifluoride (0.587 g, 3.0 mmol) was dissolved in methanol (30 ml). Then acetone (1.58 ml, 30 mmol) and zinc chloride (1.635 g, 12 mmol) were added and the reaction mixture was cooled with an ice bath. After adding sodium cyanoborohydride (0.566 g, 9.0 mmol) the mixture was allowed to stir at 40° C. overnight. After cooling, the reaction mixture was poured onto ammonium chloride/ice and extracted with ethyl acetate (2 times 50 ml). The organic layer was dried over magnesium sulfate and evaporated. The residue was purified using flash chromatography (SiO2; eluent: heptane/ethyl acetate=95:5) to yield a light yellow oil (0.530 g, 74%) that was directly used for the next step; MS (EI): 222.1 ((M-CH3)+); 237.1 (M+.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586617B2
Source datasetuspto-grants-2013_11
ORD IDord-97c7001edf2945aa9d1cc3d794721e39
Source noteuspto-grants-2013_11