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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981153Generated: November 4, 2026

Methanethiol → N-(2-Hydroxyethyl)-N-methylguanidine sulfate (2:1)

https://huagongshe.com/reaction/1981153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
ReactantIsopropanolHCID 3776—
Reactant2-(Methylamino)ethanolHCID 8016—
ReactantHCID 178485225HCID 178485225—
SolventEthanolHCID 702—
ProductN-(2-Hydroxyethyl)-N-methylguanidine sulfate (2:1)HCID 20399896—

Reaction Steps

The above intermediate N-(2-hydroxyethyl)-N-methylquanidine sulfate was prepared as follows: A mixture containing 83.6 g of methyl isothiourea sulfate and 90 g of N-(2-hydroxyethyl)methylamine was heated on a steam bath under vacuum until no more methyl mercaptan was evolved. The solid remaining was boiled successively with hot isopropyl alcohol, hot absolute ethanol and then ether, and collected to yield 91 g of crystalline N-(2-hydroxyethyl)-N-methylguanidine sulfate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04512993
Source datasetuspto-grants-1985_04
ORD IDord-f46e361758fc4810b257df44f7b9c0a6
Source noteuspto-grants-1985_04