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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369961Generated: October 30, 2026

Hydrochloric Acid → 2-Hydroxyethyl-7-nitro-1,2,3,4-tetrahydroisoquinoline hydrochloride

https://huagongshe.com/reaction/369961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthylene OxideHCID 6354—
ReactantSodium HydroxideHCID 14798—
Reactant7-Nitro-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 13521670—
SolventEthanolHCID 702—
Product2-Hydroxyethyl-7-nitro-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 2158427862%

Reaction Steps

To a solution of 7-nitro-1,2,3,4-tetrahydroisoquinoline hydrochloride (5.01 g, 23.3 mmol) in ethanol (200 ml) at 0° C. in a pressure bottle was added 2.5 M sodium hydroxide solution (10 ml). This solution was stirred for 0.2 h before ethylene oxide (4.2 ml) was added and the bottle was capped and the solution was stirred overnight while slowly allowing it to warm to ambient temperature. The solvent was concentrated and the aqueous solution was extracted twice with dichloromethane. The combined and dried (magnesium sulfate) extracts were concentrated to give an oil. This oil was immediately dissolved in ethanol (125 ml) and hydrochloric acid in ethanol was added until a distinctly acidic solution was obtained. After cooling, the title compound was collected and isolated as an off-white solid (3.76 g, 62%), m.p. 213° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140322
Source datasetuspto-grants-2000_10
ORD IDord-73a83ae02d634baa96960dccd5aa2e44
Source noteuspto-grants-2000_10