HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 67324203, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 320833 | HCID 320833 | — |
| Product | HCID 67324203 | HCID 67324203 | 86% |
Reaction Steps
A solution of (1-methyl-2-phenyl-1H-imidazol-5-yl)methanol (0.600 g, 3.19 mmol) in dry SOCl2 (11 mL) was refluxed at 80° C. for 1 h. The reaction mixture was concentrated under reduced pressure and the residue was co-evaporated with CH2Cl2, and then triturated with diethyl ether, filtered and dried under suction to afford 5-(chloromethyl)-1-methyl-2-phenyl-1H-imidazole hydrochloride (0.67 g, yield 86%) as a white solid. 1H NMR (300 MHz, MeOD) δ 7.79-7.79 (m, 6H), 4.98 (s, 2H), 3.93 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901156B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-4427e338a04041d2aad81906141105d0 |
| Source note | uspto-grants-2014_12 |