HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284186Generated: November 1, 2026
1,2-Dimethoxyethane → HCID 21515857, compound
https://huagongshe.com/reaction/1284186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Chloromethyl methyl sulfide | HCID 16916 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(2-fluorophenyl)-N'-methylurea | HCID 676515 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21515857 | HCID 21515857 | — |
Reaction Steps
A solution of 16.8 g. (0.1 mol) of N-(2-fluorophenyl)-N'-methyl urea in 250 ml. of 1,2-dimethoxyethane was cooled to 0°C. Then 4.8 g. (0.1 mol) of a 50% dispersion of sodium hydride in mineral oil was added slowly. After addition was complete, the solution was stirred for 15 minutes. This solution was added slowly to a stirred solution of 9.7 g. (0.1 mol) of chloromethyl methyl sulfide in 100 ml. of 1,2-dimethoxyethane. The resulting mixture was stirred at room temperature for 65 hours. At the end of this time, the precipitate was removed by filtration and the resulting filtrate was evaporated to give an oil which solidified upon adding water. The solid was isolated by filtration, washed with hexane and dried. Recrystallization from a hexene-benzene mixture gave 12 g. crystalline solid, melting point 102.5°-103°C. An infrared spectrum showed sharp, strong adsorptions at 3.0, 6.1, 13.05 and 13.2μ .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03978123 |
|---|
| Source dataset | uspto-grants-1976_08 |
|---|
| ORD ID | ord-2bee7b5812cc4a81bbc0e56632efe4b5 |
|---|
| Source note | uspto-grants-1976_08 |
|---|