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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083778Generated: October 26, 2026

Water → N-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosourea

https://huagongshe.com/reaction/2083778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-(2-chloroethyl)-3-(beta-D-glucopyranosyl)ureaHCID 15571360—
ReactantSodium NitriteHCID 23668193—
SolventFormic AcidHCID 284—
ProductN-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosoureaHCID 997289198.3%

Reaction Steps

A solution of 0.60 g of 1-(2-chloroethyl)-3-(β-D-glucopyranosyl)urea in 15 ml of 99% formic acid was admixed with 282 mg of sodium nitrite under ice-cooling and stirring. The mixture was stirred for 1 hour under ice-cooling to effect the nitrosation. The reaction mixture, after addition of 15 ml of cold water thereto, was ice-cooled for 30 minutes and then treated with 5 ml of Amberlite IR-120 (H+ form) for the removal of sodium cation. The reaction mixture so treated was concentrated to dryness below 30° C by distilling off the solvent under a reduced pressure. The residue was taken up into a small volume of n-propanol and the solution was admixed with a volume of petroleum ether to give precipitate. The precipitate which deposited was collected by filtration and then dried in a desiccator under vacuum, affording 0.65 g of the titled compound as an amorphous solid of pale yellow color. Yield 92%. mp. 85° C (decomposition). [α]D6 -14° (c 0.5, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04086415
Source datasetuspto-grants-1978_04
ORD IDord-2b7d926b17e1424d94ab8f606d8f1622
Source noteuspto-grants-1978_04