HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543577Generated: October 30, 2026
Dimethyl Sulfoxide → N-[(+/-)-2-[4-(2-chloro-4-trifluoromethylphenoxy)phenoxy]propionyl]isoxazolidine
https://huagongshe.com/reaction/543577
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2-Dichloro-3-(trifluoromethyl)benzene | HCID 94570 | — |
| Reactant | 2-(4-Hydroxyphenoxy)-1-(1,2-oxazolidin-2-yl)propan-1-one | HCID 13279434 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[(+/-)-2-[4-(2-chloro-4-trifluoromethylphenoxy)phenoxy]propionyl]isoxazolidine | HCID 13279435 | 96.1% |
Reaction Steps
A mixture of 1,2-dichloro-3-(trifluoromethyl)benzene (21.5 g), N-[(±)-2-(4-hydroxyphenoxy)propionyl]isoxazolidine (23.7 g) which was prepared as in Example 3, anhydrous potassium carbonate (14.5 g) and dimethylsulfoxide (200 ml) was stirred at 130° C. for 3 hours. After the mixture was cooled, water and benzene were added thereto to form two layers. The organic layer thus separated was washed with 1 N aqueous sodium hydroxide solution and then with water and dried over anhydrous sodium sulfate. Removal of the solvent by a distillation in vacuo gave N-[(±)-2-[4-(2-chloro-4-trifluoromethylphenoxy)phenoxy]propionyl]isoxazolidine (39.9 g) as a pale brown crystalline solid. Recrystallization from a mixture of n-hexane and ethyl acetate afforded a white crystalline solid. m.p. 66.5°-67.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04447259 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-f4394d3b919b4a07927fca7bb89c5bfb |
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| Source note | uspto-grants-1984_05 |
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