Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63233생성일: 2026년 10월 23일
Pentane → (2-(4-Chlorophenyl)-1-(phenylsulfonyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone
https://huagongshe.com/ko/reaction/63233
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pentane | HCID 8003 | — |
| 반응물 | Benzoyl chloride, 3,4,5-trimethoxy- | HCID 78282 | — |
| 반응물 | 2-(4-Chlorophenyl)-1-(phenylsulfonyl)-1H-imidazole | HCID 49788500 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | (2-(4-Chlorophenyl)-1-(phenylsulfonyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone | HCID 49788802 | 36.8% |
반응 단계
To a solution of 2-(4-chlorophenyl)-1-(phenylsulfonyl)-1H-imidazole (10f) (6.0 mmol) in anhydrous THF (30 mL) at −78° C. was added 1.7 M tert-butyllithium in pentane (5.3 mL, 9.0 mmol) and stirred for 10 min. 3,4,5-Trimethoxybenzoyl chloride (7.2 mmol) was added at −78° C. and stirred for overnight. The reaction mixture was diluted with 100 mL of saturated NaHCO3 solution (aqueous) and extracted by ethyl acetate (200 mL). The organic layer was dried over magnesium sulfate and concentrated. The residue was purified by flash column chromatography (hexane:ethyl acetate 4:1) to give a white solid. Yield: 36.8%; 1H NMR (500 MHz, CDCl3) δ 8.05 (d, J=7.5 Hz, 2H), 7.77 (t, J=7.5 Hz, 1H), 7.62 (t, J=8.0 Hz, 2H), 7.48 (s, 1H), 7.44 (d, J=9.0 Hz, 2H), 7.39 (d, J=8.5 Hz, 2H), 7.37 (s, 2H). MS (ESI): calculated for C25H21ClN2O6S, 512.1. found 513.1 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09447049B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-e16d5251861942d0865ec6ca7d3f8d39 |
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| 출처 메모 | uspto-grants-2016_09 |
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