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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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물1,5-Bis(3,4,5-trimethoxyphenyl)penta-1,4-dien-3-oneHCID 383405—
반응물3-Methylthio4-n-propoxy-5-benzyloxybenzaldehydeHCID 10471022—
촉매3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromideHCID 9964923—
생성물1-(3-Methylthio-4-propoxy-5-benzyloxyphenyl)4-(3,4,5-trimethoxyphenyl)butan-1,4-dioneHCID 10098743—

반응 조건

온도60 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04977146
출처 데이터셋uspto-grants-1990_12
ORD IDord-5cac2286850a4cea96c3e94dde8153df
출처 메모uspto-grants-1990_12