Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49003생성일: 2026년 10월 23일
1,4-Dioxane--water (1/1) → 5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1, 2-benzisothiazole-3-carboxaldehyde
https://huagongshe.com/ko/reaction/49003
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| 반응물 | 3-[3-(dibromomethyl)-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione | HCID 22119839 | — |
| 촉매 | Silver Nitrate | HCID 24470 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1, 2-benzisothiazole-3-carboxaldehyde | HCID 17852368 | — |
반응 단계
A solution of 3-[3-(dibromomethyl)-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione (0.500 g, 0.00100 mol) in a dioxane/water mixture (5:2) is treated with silver nitrate (0.340 g, 0.00200 mol), refluxed for 90 minutes, cooled to room temperature, stirred for 18 hrs, refluxed for three hrs, cooled, and filtered through a pad of diatomaceous earth. The resultant filtrate is concentrated in vacuo to obtain an aqueous mixture. The aqueous mixture is extracted with methylene chloride. The organic extract is washed sequentially with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a solid. Column chromatography of the solid using silica gel and methylene chloride gives the title product as a solid (0.240 g, mp 193-194.5° C.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06706663B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-6b3cd572d4d840a59b547b957ebf8cee |
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| 출처 메모 | uspto-grants-2004_03 |
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