HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(chloromethyl)-N,N-dimethylaniline hydrochloride → 2-benzylthio-4-(2-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(chloromethyl)-N,N-dimethylaniline hydrochloride | HCID 13537426 | — |
| Reactant | HCID 178418227 | HCID 178418227 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-benzylthio-4-(2-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole | HCID 18934837 | — |
Reaction Steps
Initially, 0.65 g of 2-dimethylaminobenzylchloride hydrochloride was added to a solution of 0.7 g of 2-benzylthio-5,5-dimethylimidazolin-4-thione in 20 mL of ethanol (EtOH). 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 62, and purified by column chromatography (CHCl3). Recrystallization from diethyl ether-n-hexane gave 2-benzylthio-4-(2-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole in the form of a needle-like crystal. The yield of this compound was 0.75 g with a yield ratio of 72.2%, 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-9a24f90cc7884da083a28d124bc01ed8 |
| Source note | uspto-grants-1998_03 |