HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 1-(4-Fluorophenyl)-2-(4-pyridinyl)-1,2-ethanedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-(4-Fluorophenyl)-2-(4-pyridyl)ethanediol | HCID 18771502 | — |
| Product | 1-(4-Fluorophenyl)-2-(4-pyridinyl)-1,2-ethanedione | HCID 11790992 | — |
Reaction Steps
Oxidation of 1-(4-fluorophenyl)-2-(4-pyridyl)ethanediol according to the oxalyl chloride method of Swern [J. Org. Chem., 44, p 4148, 1979)] gave the titled dione following extractive workup and recyrstallization from hexanes m.p. 85-86.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06645989B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-0a06086c93b74e6b9cae7f786da1012d |
| Source note | uspto-grants-2003_11 |