HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061440Generated: November 2, 2026
Dimethyl Sulfoxide → (4-Chloro-3-methoxy-2-pyridyl)cyclopropylketone
https://huagongshe.com/reaction/1061440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (4-Chloro-3-methoxy-2-pyridyl)-cyclopropyl-methanol | HCID 68297213 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Chloro-3-methoxy-2-pyridyl)cyclopropylketone | HCID 68297313 | 90.6% |
Reaction Steps
10.22 ml of oxalyl chloride was dissolved in 300 ml of anhydrous dichloromethane, and under cooling at −78° C., 100 ml of anhydrous dichloromethane solution of 8.95 ml of anhydrous dimethylsulfoxide was dropped thereto. The resulting mixture was stirred at −78° C. for 40 minutes, and thereafter, 200 ml of anhydrous dichloromethane solution of 19.25 g of (4-chloro-3-methoxy-2-pyridyl)cyclopropylmethane-1-ol (IX) was dropped thereto. The resulting mixture was stirred at −78° C. for 30 minutes, and thereafter, the reaction temperature was elevated to −45° C. and the resulting mixture was stirred at the same temperature for 1 hour, and thereafter, 62.79 ml of triethylamine was dropped and the temperature of the resulting mixture was elevated to a room temperature. Water was added thereto and the resulting mixture was extracted with chloroform, and the resulting organic layer was washed with water and saturated salt water, and thereafter, dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent; chloroform:ethyl acetate=20:1) to obtain 17.27 g of (4-chloro-3-methoxy-2-pyridyl)cyclopropylketone (X).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06525066B2 |
|---|
| Source dataset | uspto-grants-2003_02 |
|---|
| ORD ID | ord-2526352a7c8345d7901ad90109935454 |
|---|
| Source note | uspto-grants-2003_02 |
|---|