HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 1-Benzyl-4-chloro-5-(chloromethyl)-2(4-nitrophenyl)-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (1-benzyl-4-chloro-2-(4-nitrophenyl)-1H-imidazol-5-yl)methanol | HCID 15088539 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-Benzyl-4-chloro-5-(chloromethyl)-2(4-nitrophenyl)-imidazole | HCID 22345725 | — |
Reaction Steps
Thionyl chloride (0.90 ml, 1.48 g, 12.4 mmol) was added dropwise to a stirred suspension of 1-benzyl-4-chloro-5-(hydroxymethyl)-2(4-nitrophenyl)imidazole (18.5 g, 5.4 mmole) in chloroform (15 ml) at room temperature. The brown solution was stirred for 2.5 hours then evaporated to dryness. Toluene (12 ml) was added to the residue and evaporated to dryness. The residue was dissolved in chloroform (20 ml) and used in the next step for introduction of the cyano functional group.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06921525B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-aea224c8f7c4441386cb5c1a4fd77751 |
| Source note | uspto-grants-2005_07 |