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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569977Generated: October 30, 2026

Phenylethanolamine → HCID 13713311, compound

https://huagongshe.com/reaction/569977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylethanolamineHCID 1000—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-(4-Nitrophenyl)butan-2-oneHCID 12235672—
ReactantHCID 13713312HCID 13713312—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 13713311HCID 13713311—

Reaction Steps

A solution of 5.0 g. (25.9 mM) of 2-amino-1-phenylethanol and 3.55 g. (25.9 mM) of methyl 2-(4-nitrophenyl)ethyl ketone in 60 ml. of toluene containing 10 mg. of para-toluenesulfonic acid was heated at reflux for six hours in a flask equipped with a Dean-Stark trap. The water that formed during the reaction was removed via the trap, and then the reaction mixture was cooled to room temperature and concentrated to dryness by evaporation of the solvent under reduced pressure. The solid product that remained was dissolved in 50 ml. of tetrahydrofuran and the solution was heated to reflux. A solution of 13.5 ml. of 2N borane-methyl sulfide complex in tetrahydrofuran was then added dropwise to the reaction mixture, and the mixture was refluxed for an additional ninety minutes. After cooling the reaction mixture to room temperature, it was diluted by addition of diethyl ether saturated with hydrogen chloride. The precipitate that formed was collected by filtration and crystallized from ethanol and diethyl ether to give 3.29 g. of 1-phenyl-2 -[1-methyl-3-(4-nitrophenyl)propylamino]ethanol hydrochloride. M.P. 203-213° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734437
Source datasetuspto-grants-1988_03
ORD IDord-ca764e040de54189bcdbddb9058b57d8
Source noteuspto-grants-1988_03