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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763556Generated: October 31, 2026

Hydroxyamine hydrochloride → HCID 178513441, compound

https://huagongshe.com/reaction/1763556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantPotassium ethoxideHCID 23670592—
ReactantHCID 178504053HCID 178504053—
SolventEthanolHCID 702—
ProductHCID 178513441HCID 178513441—

Reaction Steps

10 g of 1-(indolin-1-yl)-2-methylisothiourea hydrochloride and 11.4 g of hydroxylamine hydrochloride were suspended in 240 ml of ethanol and were heated to the boil for one hour upon the addition of 6.9 g of potassium ethoxide. Upon cooling, the potassium chloride and the excess hydroxylamine hydrochloride were filtered off with suction and the filtrate was evaporated to dryness. The evaporation residue was partitioned between concentrated aqueous ammonia solution and methylene choride. The methylene chloride solution was dried over magnesium sulphate and evaporated to dryness. 1-hydroxy-3-(indolin-1-yl)guanidine was obtained as an evaporation residue and was crystallized upon the addition of acetic acid, as the acetate from ethanol/ether having a M.Pt. of 155° - 156°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112111
Source datasetuspto-grants-1978_09
ORD IDord-f6bbb17747c04149b8a710116a7f9e60
Source noteuspto-grants-1978_09