HuagongsheHuagongshe Chemistry Print Report · For research reference only
5,5-Dimethyl-2,4-imidazolidinedithione → 2,4-bis(3-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5,5-Dimethyl-2,4-imidazolidinedithione | HCID 3002142 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3-(chloromethyl)-N,N-dimethylaniline hydrochloride | HCID 18934895 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,4-bis(3-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole | HCID 18934902 | — |
Reaction Steps
Initially, 2.94 g of 3-dimethylaminobenzylchloride hydrochloride was added to a mixture of 1.6 g of 5,5-dimethyl-2,4-dithiohydantoin and 1.3 g of sodium methoxide in 50 mL of methanol (MeOH). The reaction mixture was stirred at the room temperature for one hour, and concentrated in vacuo. The residue was treated following the procedure used in Example 56, and chromatographed on a column of silica gel (CHCl3). From the earlier fractions, 2,4-bis(3-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole was isolated, in the form of a syrup. The yield of this compound was 0.31 g with a yield ratio of 7.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05733922 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-483dd6c046dd4bfda158d9c42f0f2afc |
| Source note | uspto-grants-1998_03 |