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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1-(2-chloroethyl)-3-(beta-D-glucopyranosyl)urea | HCID 15571360 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | N-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosourea | HCID 9972891 | 98.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04086415 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-2b7d926b17e1424d94ab8f606d8f1622 |
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| Source note | uspto-grants-1978_04 |
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