Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1085635생성일: 2026년 10월 26일
Dimethylformamide → 1-(5-Iodo-4-hydroxy-3-methoxyphenyl)-4-(3,4,5-trimethoxyphenyl)butan-1,4-dione
https://huagongshe.com/reaction/1085635
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1,5-Bis(3,4,5-trimethoxyphenyl)penta-1,4-dien-3-one | HCID 383405 | — |
| 반응물 | 3-Iodo-5-methoxy-4-[(trimethylsilyl)oxy]benzaldehyde | HCID 15718025 | — |
| 촉매 | 3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide | HCID 9964923 | — |
| 생성물 | 1-(5-Iodo-4-hydroxy-3-methoxyphenyl)-4-(3,4,5-trimethoxyphenyl)butan-1,4-dione | HCID 15718033 | — |
반응 단계
To 3-iodo-4-trimethylsilyloxy-5-methoxybenzaldehyde in 570 mL of seive dried DMF was added 3,4,5-trimethoxyphenylvinyl ketone from Example 1, Step B (179 g, 0.805 mole) and 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide (61.9 g, 0.24 mole). Triethylamine (320 mL) was added, and the resulting mixture was stirred at 70° C. under nitrogen atmosphere for 2 hours. The mixture was cooled, filtered, and washed with MeOH (500 mL). The resulting solution was cautiously acidified with 6 N HCL to pH 1.5 and a heavy yellow precipitate began to form. This mixture was stirred at room temperature for 2 hours to ensure complete desilylation. The precipitate was filtered, washed with H2O (4×1 L), and redissolved in a minimum volume of CH2Cl2. The solution was washed with brine, dried over anhydrous MgSO4, and evaporated in vacuo to provide a white solid. The solid was washed with MeOH and dried under high vacuum to provide 1-(5-iodo-4-hydroxy-3-methoxyphenyl)-4-(3,4,5-trimethoxyphenyl)butan-1,4-dione as a white solid, m.p. 189°-190° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05010100 |
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| 출처 데이터셋 | uspto-grants-1991_04 |
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| ORD ID | ord-e9e309b1568243468fa200e65eddd2da |
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| 출처 메모 | uspto-grants-1991_04 |
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