Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1110821생성일: 2026년 10월 24일
Hydrochloric Acid → 1-(3-Methylthio-4-propoxy-5-benzyloxyphenyl)4-(3,4,5-trimethoxyphenyl)butan-1,4-dione
https://huagongshe.com/ko/reaction/1110821
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 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-Methylthio4-n-propoxy-5-benzyloxybenzaldehyde | HCID 10471022 | — |
| 촉매 | 3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide | HCID 9964923 | — |
| 생성물 | 1-(3-Methylthio-4-propoxy-5-benzyloxyphenyl)4-(3,4,5-trimethoxyphenyl)butan-1,4-dione | HCID 10098743 | — |
반응 단계
3-methylthio-4-n-propoxy-5-benzyloxybenzaldehyde, 135 g of 3,4,5-trimethoxyphenylvinylketone, 10 g of 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazoliumbromide, 25 mL of triethyl amine dissolved in 150 ml of dimethylformamide was heated at 60° C. overnight, and the reaction mixture was treated with 400 mL of 1.5N HCl and the aqueous layer decanted. The residue was treated again with fresh 400 mL of 1.5N HCl and decanted two more times. The remaining residue was crystallized from 400 mL of methanol and washed thoroughly with methanol, hexane, and methanol and dried to yield the title compound as a tan solid: NMR(200 MHz, CDCl3) δ 1.03(t, CH2CH2CH3), 1.82(m, CH2CH2CH3), 2.50(s, SCH3), 3.43(s, C(O)CH2CH2CO, 3.94(s, 3 OCH3), 4.11 (t, OCH2CH2CH3), 5.17(s, OCH2Ar), 7.30-7.52(m, ArH).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04977146 |
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| 출처 데이터셋 | uspto-grants-1990_12 |
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| ORD ID | ord-5cac2286850a4cea96c3e94dde8153df |
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| 출처 메모 | uspto-grants-1990_12 |
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