HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023469Generated: October 26, 2026
Dimethyl Sulfoxide → 2-(4-Fluorophenyl)cyclohexan-1-one
https://huagongshe.com/reaction/1023469
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 20487437 | HCID 20487437 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Fluorophenyl)cyclohexan-1-one | HCID 13089540 | 69.2% |
Reaction Steps
To a solution of oxalyl chloride (0.45 mL, 5.2 mmol) in dry dichloromethane (15 mL) at −78° C. is added a solution of DMSO (0.73 mL, 10.3 mmol) in dichloromethane (10 mL) dropwise, and the resulting mixture is allowed to stir at −78° C. for 30 minutes. Then a solution of 2-(4-Fluoro-phenyl)-cyclohexanol (500 mg, 2.57 mmol) in dichloromethane (5 mL) is added and stirred for 15 minutes. Then triethylamine (2.87 mL, 15.4 mmol) is added and the reaction is allowed to slowly warm up to 20° C. and stirred for 16 hours. The mixture is poured into ice-water (30 mL) and organic layer is washed with water (10 mL×5), then brine (10 mL×1) and dried over anhdrous sodium sulfate. After concentration, the crude is purified by silica flash column chromatography using EtOAc in Heptane (gradient from 0% to 30%) to give 342 mg of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08722709B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-c512da44ff1a4f44953c783a1409dfd6 |
|---|
| Source note | uspto-grants-2014_05 |
|---|