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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923Generated: October 26, 2026

4-(2-Oxopropoxy)benzonitrile → 2-(4-Cyanophenoxy)-1-methylethylamine

https://huagongshe.com/reaction/923

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Oxopropoxy)benzonitrileHCID 309603—
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
Product2-(4-Cyanophenoxy)-1-methylethylamineHCID 1897279927.8%

Reaction Steps

293 g of ammonium acetate and 16.7 g of sodium cyanoborohydride were added to a solution containing 66.5 g of 4-cyanophenoxyacetone dissolved in 1500 mL of methanol, and the resultant mixture was stirred for 30 hours at room temperature. The reaction mixture was then concentrated under reduced pressure, and acidified with concentrated hydrochloric acid. 500 mL of diethyl ether and 300 mL of water were then added thereto. Subsequently, the resultant water layer was made basic with a 5% aqueous solution of sodium hydroxide, the solution was extracted with 1000 mL of diethyl ether, and then washed with water. The organic layer was then dried over anhydrous sodium sulfate, and the diethyl ether was removed under reduced pressure. The obtained residue was distilled under reduced pressure to yield 13.0 g of the desired product (19%). Boiling point: 132° C./0.26 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723469
Source datasetuspto-grants-1998_03
ORD IDord-a811a98a5e964e1b95e931e2733e70ca
Source noteuspto-grants-1998_03