Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247464Generated: October 30, 2026

Hydrochloric Acid → HCID 20160887, compound

https://huagongshe.com/reaction/247464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenylethanolamineHCID 1000—
Reactant6-Methoxy-1,2,3,4-tetrahydronaphthalen-2-oneHCID 75582—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventIsopropanolHCID 3776—
ProductHCID 20160887HCID 2016088747.5%

Reaction Steps

An amount of 4 g of 6-methoxy-2-tetralone is reacted at 35° C. for 3 hours with 3.2 g of 2-amino-1-phenylethanol in 100 ml of methanol and 4 ml of glacial acetic acid in the presence of hydrogen and 0.3 g of platinum bioxide. After filtration and concentration, the residue is taken up with sodium hydroxide and extracted with ethyl acetate. The solution is dried over anhydrous sodium sulfate and evaporated. The black oil thus obtained is purified by flash-chromatography by utilizing a mixture of methylene chloride/methanol 9/1 as eluant. The fractions containing the product are collected and evaporated to dryness. The residue is dissolved in 20 ml of isopropyl alcohol and to the solution thus obtained there is added a saturated solution of hydrogen chloride in isopropyl alcohol. Thus, there is obtained the 2-[(6-methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochloride, designated by its code number SR 58280 A, which, after crystallization from isopropyl alcohol, melts at 174°-176° C. Yield: 47.5% of the theoretical value.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04707497
Source datasetuspto-grants-1987_11
ORD IDord-86a8cbfb8c8d4ce1a9bb3787ca08f21a
Source noteuspto-grants-1987_11