HuagongsheHuagongshe Chemistry Print Report · For research reference only
5,5-Dimethyl-2,4-imidazolidinedithione → 2,4-bis-(4-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5,5-Dimethyl-2,4-imidazolidinedithione | HCID 3002142 | — |
| Reactant | 4-(chloromethyl)-N,N-dimethylaniline hydrochloride | HCID 18934874 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,4-bis-(4-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole | HCID 18934841 | — |
Reaction Steps
Initially, 3.2 g of 4-dimethylaminobenzylchloride hydrochloride was added to a solution of 1 g of 5,5-dimethyl-2,4-dithiohydantoin in 50 mL of ethanol (EtOH). The reaction mixture was treated following the procedure used in Example 62, and purified by column chromatography (CHCl3). Recrystallization form diethyl ether-n-hexane gave the desired compound in the form of a needle-like crystal. The yield of this compound was 1.9 g with a yield ratio of 71.2%, and the melting point was 91°-92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05733922 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-6f30ba70e6f749ca9b50c7fefb87d362 |
| Source note | uspto-grants-1998_03 |