HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763556Generated: October 31, 2026
Hydroxyamine hydrochloride → HCID 178513441, compound
https://huagongshe.com/reaction/1763556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Potassium ethoxide | HCID 23670592 | — |
| Reactant | HCID 178504053 | HCID 178504053 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178513441 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04112111 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-f6bbb17747c04149b8a710116a7f9e60 |
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| Source note | uspto-grants-1978_09 |
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