Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1172697생성일: 2026년 10월 27일
Water → 2,5-Difluoro-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-benzonitrile
https://huagongshe.com/reaction/1172697
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Water | HCID 962 | — |
| 반응물 | 2,4,5-Trifluorobenzonitrile | HCID 593813 | — |
| 반응물 | 1-[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propan-1-ol | HCID 23549129 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | tert-Butanol | HCID 6386 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2,5-Difluoro-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-benzonitrile | HCID 59556309 | 95.5% |
반응 단계
To a solution of 900 mg of 1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propan-1-ol in 2 mL of tetrahydrofuran at 5° C. was slowly added 3.3 mL of a molar solution of potassium tert-butoxide in tert-butanol. After stirring at 5° C. for 30 minutes, the resulting solution was slowly added to a solution of 469 mg of 2,4,5-trifluoro-benzonitrile in 2 mL of tetrahydrofuran at −60° C. The resulting mixture was stirred for 1 h at −60° C. then stirred overnight allowing the temperature to warm up to room temperature. It was then poured into water and extracted with dichloromethane. The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel (gradient from heptane 100 to heptane 80/ethyl acetate 20) to give 1.25 g of 2,5-difluoro-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-benzonitrile.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07834030B2 |
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| 출처 데이터셋 | uspto-grants-2010_11 |
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| ORD ID | ord-640d9a37120e4412a9ff258c71214264 |
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| 출처 메모 | uspto-grants-2010_11 |
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