HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583946Generated: October 31, 2026
1,3-Dimethyl-2-imidazolidinone → HCID 12074072, compound
https://huagongshe.com/reaction/583946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | HCID 12074071 | HCID 12074071 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Solvent | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Product | HCID 12074072 | HCID 12074072 | — |
Reaction Steps
To a solution of the compound prepared in Example 4 (1.87 g) and 1,3-dimethyl-2-imidazolidinone (1.7 ml) in tetrahydrofuran (THF; 20 ml), 1M lithium bis(trimethylsilyl)amide (11.4 ml; in THF) was dropped at −78° C., and then the mixture was stirred for 30 minutes at same temperature. Methoxymethyl chloride (1.2 ml) was added to the reaction mixture, and the mixture was stirred for 3 hours. The reaction mixture was diluted with a saturated aqueous solution of ammonium chloride, and warmed to room temperature, and then the solution was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated. The residue was purified by column chromatography (toluene:ethyl acetate=2:1) to give the title compound (1.45 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06924307B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-c5fb17d1392b432ea5c14bb64a7e100f |
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| Source note | uspto-grants-2005_08 |
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