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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158077Generated: October 30, 2026

Ethanol → 2-(2-Chlorophenyl)propan-2-amine

https://huagongshe.com/reaction/1158077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydrogen PeroxideHCID 784—
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-chlorophenyl)-2-MethylpropanenitrileHCID 9815403—
SolventWaterHCID 962—
Product2-(2-Chlorophenyl)propan-2-amineHCID 10535147—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(2-Chlorophenyl)-2-methylpropanenitrile (5.0 g, 0.028 mol) along with 50 mL of EtOH was added into a 250 mL round-bottomed flask. To this was added 50 mL of saturated aqueous K2CO3. This mixture was cooled to 0° C. then 85 mL of 30% aqueous H2O2 was slowly added. The reaction mixture was allowed to warm to room temperature, and then it was stirred at that temperature for 12 h. The mixture was extracted with CH2Cl2 (3×150 mL), and the combined organic extracts were dried over MgSO4, filtered, and concentrated in vacuo to give a viscous oil. To this oil was added 40 mL of CH3CN, 40 mL H2O, and 13.2 g (0.031 mol) of PhI(O2CCF3)2. This mixture was stirred at r.t. for 12 h, diluted with 300 mL of H2O, and then stirred for an additional 4 h at room temperature. The aqueous phase was extracted using MTBE (1×200 mL) follow by diethyl ether (2×100 mL). The aqueous layer was basified with 1N NaOH (pH=13) and then extracted with CH2Cl2 (3×100 mL). The organic extracts were dried and concentrated in vacuo to give the desired product as a colorless oil that was used in subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807700B2
Source datasetuspto-grants-2010_10
ORD IDord-997c646a6ece4b7d8cca620d960e33bd
Source noteuspto-grants-2010_10