Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 864266생성일: 2026년 10월 27일
2-Bromo-3-fluoro-5-(4-octyloxyphenyl)pyrazine → 2-Fluoro-3-octyl-6-(4-octyloxyphenyl)pyrazine
https://huagongshe.com/reaction/864266
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Bromo-3-fluoro-5-(4-octyloxyphenyl)pyrazine | HCID 21804633 | — |
| 반응물 | HCID 178443577 | HCID 178443577 | — |
| 촉매 | HCID 178418745 | HCID 178418745 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Fluoro-3-octyl-6-(4-octyloxyphenyl)pyrazine | HCID 19418296 | — |
반응 단계
7.95 mmol of freshly prepared octylmagnesium bromide in 30 ml of tetrahydrofuran are added dropwise at -10° C. to 2.00 g (5.3 mmol) of 2-bromo-3-fluoro-5-(4-octyloxyphenyl)pyrazine and 0.03 g (0.06 mmol) of [1,3-bis-(diphenylphosphino)propane]nickel(II) chloride in 30 ml of tetrahydrofuran, and the reaction mixture is stirred overnight, during which it warms to room temperature. The reaction mixture is partitioned between aqueous ammonium chloride solution and ether, the organic phase is washed with aqueous sodium chloride solution, dried over sodium sulfate, filtered and freed from the solvent, and the mixture is purified by chromatography (silica gel/dichloromethane: hexane = 7:3). 1.12 g of 2-fluoro-3-octyl-6-(4-octyloxyphenyl)pyrazine are obtained. ##STR17## The compound has the following phase sequence:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05562859 |
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| 출처 데이터셋 | uspto-grants-1996_10 |
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| ORD ID | ord-acb452673ccb482b9d8959684f9ae9c6 |
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| 출처 메모 | uspto-grants-1996_10 |
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