HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Ethyl 2-[4-(chloromethyl)phenyl]-1,3-oxazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Ethyl 2-[4-(hydroxymethyl)phenyl]-1,3-oxazole-4-carboxylate | HCID 46834789 | — |
| Reactant | HCID 178418385 | HCID 178418385 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-[4-(chloromethyl)phenyl]-1,3-oxazole-4-carboxylate | HCID 46834790 | 82% |
Reaction Steps
A solution of ethyl 2-[4-(hydroxymethyl)phenyl]-1,3-oxazole-4-carboxylate (0.467 g, 1.89 mmol) in CH2Cl2 was treated with a solution of thionyl chloride (0.281 g, 2.36 mmol) and benzotriazole (0.281 g, 2.36 mmol) in CH2Cl2, and stirred 6 hours at room temperature. The reaction was diluted with CHCl3, filtered over Celite and concentrated under vacuum. The resultant residue was purified by flash chromatography (silica, MeOH:CH2Cl2 5%) to give the title product in 82% yield, identified by NMR and mass spectral analyses. LCMS (ESI+) 266 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803825B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-f149aedecfa84eb0a80e0ed0eacee0a5 |
| Source note | uspto-grants-2010_09 |