HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → N-(2-Hydroxyethyl)-N-methylguanidine sulfate (2:1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 2-(Methylamino)ethanol | HCID 8016 | — |
| Reactant | HCID 178485225 | HCID 178485225 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04512993 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-f46e361758fc4810b257df44f7b9c0a6 |
| Source note | uspto-grants-1985_04 |