HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-[2-(4-Chloromethylphenoxy)ethyl]-5-methyl-2-phenyloxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzyl alcohol | HCID 11833828 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-[2-(4-Chloromethylphenoxy)ethyl]-5-methyl-2-phenyloxazole | HCID 11809594 | 90.2% |
Reaction Steps
To a solution of 4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzyl alcohol (6.8 g) in chloroform (100 ml) was added thionyl chloride (3.1 g), and the mixture was stirred for one hour at room temperature. The reaction mixture was washed with a saturated aqueous solution of sodium hydrogencarbonate and then water, followed by drying (MgSO4). The solvent was distilled off to leave 4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzyl chloride (6.5 g, 90%) as colorless needles, m.p.93°-94° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05591862 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-01f8fcbfc83d407e8a9dcfa60ac58dcc |
| Source note | uspto-grants-1997_01 |