Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 917381생성일: 2026년 10월 26일
Dimethylformamide → 4,4-Difluoro-3-methyl-3-butenyl 4-methyl-2-phenylthiazole-5-carboxylate
https://huagongshe.com/reaction/917381
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 4-Methyl-2-phenyl-thiazole-5-carboxylic acid | HCID 720957 | — |
| 반응물 | 4,4-Difluoro-3-Methyl-3-Buten-1-Yl Methanesulfonate | HCID 23020237 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4,4-Difluoro-3-methyl-3-butenyl 4-methyl-2-phenylthiazole-5-carboxylate | HCID 69178921 | 94% |
반응 단계
To 25 ml of N,N-dimethylformamide were dissolved 2.60 g (13 mmol) of 4,4-difluoro-3-methyl-3-butenyl methanesulfonate and 2.19 g (10 mmol) of 4-methyl-2-phenylthiazole-5-carboxylic acid, followed by the addition of 1.68 g (20 mmol) of sodium hydrogencarbonate and stirring at 100° C. for 3 hours. The reaction liquid was then poured in water and extracted with diethyl ether. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentration under reduced pressure. The residue was purified with silica gel column chromatography (ethyl acetate ether: hexane=1:9) to obtain 3.03 g (yield: 94%) of 4,4-difluoro-3-methyl-3-butenyl 4-methyl-2-phenylthiazole-5-carboxylate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07273878B2 |
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| 출처 데이터셋 | uspto-grants-2007_09 |
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| ORD ID | ord-c74a8cac6b1e46f7bf1fc4135f11063b |
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| 출처 메모 | uspto-grants-2007_09 |
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