HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(Chloromethyl)-5-(4-chlorophenyl)-1,3-oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | [5-(4-Chlorophenyl)-1,3-oxazol-4-yl]methanol | HCID 58284362 | — |
| Product | 4-(Chloromethyl)-5-(4-chlorophenyl)-1,3-oxazole | HCID 58284264 | — |
Reaction Steps
269 mg (0.77 mmol) of the compound from Example 38A are initially charged in 0.43 ml (5.85 mmol) of thionyl chloride. The reaction mixture is stirred at RT for 12 h, and excess thionyl chloride is then removed under reduced pressure. The residue is taken up in 5 ml of ethyl acetate and washed once with 2 ml of sat. aqueous sodium bicarbonate solution. The organic phase is dried over magnesium sulfate and the solvent is removed on a rotary evaporator. The product obtained is used without further purification in the subsequent reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09095582B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-73aa8356cf0b45e293dc9bff575be878 |
| Source note | uspto-grants-2015_08 |