Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 703038생성일: 2026년 10월 26일
Tetrahydrofuran → 3-[2-Methyl-3,4-dihydro-3-oxo-4-(propynyl)-2H-1,4-benzoxazin-6-yl]-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione
https://huagongshe.com/reaction/703038
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Ethyl 3-amino-4,4,4-trifluoro-2-butenoate | HCID 136209 | — |
| 반응물 | 6-isocyanato-2-methyl-3,4-dihydro-3-oxo-4-(2-propynyl)-2H-1,4-benzoxazine | HCID 15029563 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 3-[2-Methyl-3,4-dihydro-3-oxo-4-(propynyl)-2H-1,4-benzoxazin-6-yl]-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione | HCID 22151123 | — |
반응 단계
A slurry of 1.4 g. of sodium hydride in 25 ml. of dry tetrahydrofuran (THF) was cooled to -10° C. To the cooled and stirred slurry was added a solution of 10.0 g. of ethyl 3-amino-4,4,4-trifluoro-2-butenoate in 50 ml. of THF. The addition of this solution was made over a period of 30 minutes. The resultant light brown reaction mixture was cooled to -70° C. A solution of 13.3 g. of 6-isocyanato-2- methyl-3,4-dihydro-3-oxo-4-(2-propynyl)-2H-1,4-benzoxazine in 75 ml. of THF was added to the chilled reaction mixture over a period of 10 minutes. After stirring at -70° C. for 30 minutes, the temperature was allowed to rise slowly to 10° C. At that point 3.6 ml. of acetic acid was added to the mixture. A beige solid precipitated. 19.0 Grams of the solid was recovered by filtering it from the reaction mixture.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04981508 |
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| 출처 데이터셋 | uspto-grants-1991_01 |
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| ORD ID | ord-d05d21b41e2b446ba3921ae65d778a14 |
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| 출처 메모 | uspto-grants-1991_01 |
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