HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 68663368, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 68664421 | HCID 68664421 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 68663368 | HCID 68663368 | — |
Reaction Steps
To a solution of [4-[5-(5-methyl-1,3,4-oxadiazol-2-yl)-1-benzofuran-3-yl]phenyl]methanol (204 mg, 0.66 mmol) in 1,2-dichloroethane (5 mL) was added thionyl chloride (0.240 mL, 3.33 mmol), and the resulting mixture was heated under reflux for 1 hr. After cooling, the reaction mixture was concentrated under reduced pressure to give crude 2-[3-[4-(chloromethyl)phenyl]-1-benzofuran-5-yl]-5-methyl-1,3,4-oxadiazole as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492378B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-dc889ca4f1f1489e99dbb3d0c1c2a867 |
| Source note | uspto-grants-2013_07 |