Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051856Generated: October 31, 2026

3-Chloro-1,2-propanediol → HCID 20378122, compound

https://huagongshe.com/reaction/2051856

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-1,2-propanediolHCID 7290—
Reactant2-Chloroethyl isocyanateHCID 16035—
ReactantHCID 20378142HCID 20378142—
ReactantMonomethylamine methanolHCID 57454252—
SolventMethanolHCID 887—
SolventTriethylamineHCID 8471—
ProductHCID 20378122HCID 2037812256%

Reaction Steps

A mixture of 3.3 g of 3-chloro-1,2-dihydroxy-n-propane and 20 ml of 30% methylamine-methanol solution is allowed to stand at room temperature for 3 days. The reaction mixture is condensed to dryness under reduced pressure, whereby 4.2 g of N-methyl-2,3-dihydroxy-n-propylamine hydrochloride are obtained as a crude product. 4.2 g of said crude product and 3 g of triethylamine are dissolved in 30 ml of methanol. To the solution, 3.2 g of 2-chloroethyl isocyanate are added dropwise to the solution at 0° to 5° C. The solution is stirred at room temperature for 2 hours. Then, the reaction solution is condensed under reduced pressure and the residue thus obtained is purified by silica gel chromatography (Solvent: chloroform-ethyl acetate-methanol(3:1:1)). 3.5 g of 1-(2-chloroethyl)-3-methyl-3-(2,3-dihydroxy-n-propyl)urea are obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04182757
Source datasetuspto-grants-1980_01
ORD IDord-b82007a69a2147eaa96c3241c3a5645d
Source noteuspto-grants-1980_01