Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1199617생성일: 2026년 10월 25일
Potassium Carbonate → 6-fluoro-3-(5-methyl-1,2,4-oxadiazol-3-ylmethyl)-2(3H)-benzothiazolone
https://huagongshe.com/reaction/1199617
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Benzothiazolinone, 6-fluoro- | HCID 44667 | — |
| 반응물 | 3-(Chloromethyl)-5-methyl-1,2,4-oxadiazole | HCID 302157 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 6-fluoro-3-(5-methyl-1,2,4-oxadiazol-3-ylmethyl)-2(3H)-benzothiazolone | HCID 19979499 | 91.3% |
반응 단계
A mixture of 6-fluoro-2(3H)-benzothiazolone (8.45 g), acetonitrile (100 ml) and potassium carbonate (7.6 g) was prepared. To this mixture was added dropwise 3-chloromethyl-5-methyl-1,2,4-oxadiazole (7.3 g) at a temperature of 40° to 50° C. under stirring. The reaction mixture was heated under refluxing for 5 hours. The reaction mixture was then cooled and filtered. The filtrate was distilled under a reduced pressure, and the residue was admixed with ethyl acetate (200 ml) and water (100 ml). The resultant organic layer was separated and washed with a 5% aqueous potassium hydroxide solution, with water and then with a saturated aqueous sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was dissolved in a minimum amount of ethanol under heating. The solution thus formed was cooled to a temperature of 0° to 5° C. to precipitate a crystalline product, which was then separated by filtration, and dried, so that the aimed compound, i.e. 6-fluoro-3-(5-methyl-1,2,4-oxadiazol-3-ylmethyl)-2(3H)-benzothiazolone (12.1 g) was obtained. m.p. 142°-144° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04902335 |
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| 출처 데이터셋 | uspto-grants-1990_02 |
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| ORD ID | ord-b37db02ce37646279c0747d2377c47be |
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| 출처 메모 | uspto-grants-1990_02 |
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