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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977109Generated: November 1, 2026

Ethanol → HCID 136133141, compound

https://huagongshe.com/reaction/977109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl AcetateHCID 8857—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantN-Nitro-S-methylisothioureaHCID 135927615—
ProductHCID 136133141HCID 136133141—

Reaction Steps

The thus obtained crude oily substance was mixed with 3.07 g of S-methyl-N-nitroisothiourea, 0.1 g of dimethylaminopyridine (DMAP) and 30 ml of ethanol, and the mixture was refluxed. After the completion of reaction, ethyl acetate was added, and insolubles were then removed by filtration. The filtrate was concentrated under a reduced pressure to precipitate crystals, and the thus precipitated crystals were then removed by filtration. Next, the filtrate was concentrated under a reduced pressure to obtain an oily substance, and this oily substance was then purified by silica gel column chromatography (1:2 acetone/ethyl acetate) to obtain 1.04 g of 1-[(tetrahydro-3-furanyl)methyl]-2-(nitroimino)imidazolidine as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614527
Source datasetuspto-grants-1997_03
ORD IDord-7eb93f9bb7d946b3aedc86a61ab64582
Source noteuspto-grants-1997_03