Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637839Generated: October 29, 2026

Hydrazine hydrate (1:1) → 2-(3,5-Dichlorophenoxy)ethanamine hydrochloride (1:1)

https://huagongshe.com/reaction/637839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 7571580HCID 7571580—
SolventEthanolHCID 702—
Product2-(3,5-Dichlorophenoxy)ethanamine hydrochloride (1:1)HCID 7536644943.2%

Reaction Steps

A mixture of 105.5 g (0.31 mole) of 2-[2-(3,5-dichlorophenoxy)ethyl]-1H-isoindole-1,3-(2H)-dione and 24.5 (0.41 mole) 85% hydrazine hydrate in 1 liter of 95% ethanol was heated at reflux for 4 hr. A white solid was filtered off and discarded. The filtrate was stripped to dryness and the residue partitioned between water and chloroform. The chloroform layer was washed with aqueous 10% sodium hydroxide solution and then extracted with 1N sulfuric acid. The aqueous acidic layer was made alkaline and extracted with chloroform. The chloroform layer was dried over magnesium sulfate and evaporated to obtain an oil, the free base of the title compound. A portion of the oil was reacted with ethereal hydrogen chloride to give white crystalline product in 43.2% yield, m.p. 229°-231° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04558155
Source datasetuspto-grants-1985_12
ORD IDord-ce16cfd24c8045db9253e62a8839baf5
Source noteuspto-grants-1985_12