HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzoyl chloride → (4-Fluorophenyl)-2-thiazolylmethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | 2-Trimethylsilylthiazole | HCID 588453 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Fluorophenyl)-2-thiazolylmethanone | HCID 2758956 | 77.9% |
Reaction Steps
4-fluorobenzoyl chloride (3 mL, 25.4 mmol) was added to 2-(trimethylsilyl)thiazole (2 mL, 12.7 mmol) in dichloromethane (70 mL). The reaction mixture was stirred over night at rt. Dichloromethane was evaporated under reduced pressure, and the crude product purified on a normal phase silica-gel column with 0-40% ethyl acetate in hexane to afford the title compound as white amorphous solid (2.050 g, 77% yield); MS (M+H)+ 208.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858785B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-39c22c79ae9b4a3ab1cd2e8f25e943bf |
| Source note | uspto-grants-2010_12 |