Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 452560생성일: 2026년 10월 26일
Chlorotrimethylsilane → 2-bromo-1-(4-fluoro-5-methoxy-1-{[6-(trifluoromethyl)pyridin-3-yl]methyl}-2,3-dihydro-1H-inden-1-yl)ethanone
https://huagongshe.com/reaction/452560
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| 반응물 | 1-(4-fluoro-5-methoxy-1-{[6-(trifluoromethyl)pyridin-3-yl]methyl}-2,3-dihydro-1H-inden-1-yl)ethanone | HCID 66923534 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-bromo-1-(4-fluoro-5-methoxy-1-{[6-(trifluoromethyl)pyridin-3-yl]methyl}-2,3-dihydro-1H-inden-1-yl)ethanone | HCID 86650848 | — |
반응 단계
1-(4-fluoro-5-methoxy-1-{[6-(trifluoromethyl)pyridin-3-yl]methyl}-2,3-dihydro-1H-inden-1-yl)ethanone (600 mg, 1.6 mmol) was diluted in THF (3 ml). This solution was cooled to −78° C. and Sodium bis(hexamethylsilyl) amide (1.8 ml, 1.8 mmol) was added. After stirring for 10 min, chloro trimethylsilane (230 μl, 1.8 mmol) was added drop wise at −78° C., after which the reaction was warmed to 0° C., and left stirring for 30 min. To this solution was added Phenyltrimethylammonium tribromide (680 mg, 1.8 mmol) portion wise, and THF (1 mL) was added for solubility purposes. The reaction mixture was allowed to warm to room temp. Aqueous work up, extracted with dichloromethane, dried over magnesium sulfate, filtered, concentrated under reduced pressure furnished 2-bromo-1-(4-fluoro-5-methoxy-1-{[6-(trifluoromethyl)pyridin-3-yl]methyl}-2,3-dihydro-1H-inden-1-yl)ethanone. Used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08492387B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-c4e9f792eaf9460f947e7829531bd227 |
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| 출처 메모 | uspto-grants-2013_07 |
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