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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloro-1,2-propanediol | HCID 7290 | — |
| Reactant | 2-Chloroethyl isocyanate | HCID 16035 | — |
| Reactant | HCID 20378142 | HCID 20378142 | — |
| Reactant | Monomethylamine methanol | HCID 57454252 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20378122 | HCID 20378122 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04182757 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-b82007a69a2147eaa96c3241c3a5645d |
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| Source note | uspto-grants-1980_01 |
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