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HRID 552283생성일: 2026년 10월 26일

3-Chloro-4-hydroxy-5-methoxybenzaldehyde → 3-(3-Chloro-4-hydroxy-5-methoxy-phenyl)-1-(5-ethyl-4-phenyl-thiophen-2-yl)-propan-1-one

https://huagongshe.com/reaction/552283

반응식

참여 물질

역할이름HCID투입량
반응물3-Chloro-4-hydroxy-5-methoxybenzaldehydeHCID 29622—
반응물1-(5-Ethyl-4-phenyl-thiophen-2-yl)-ethanoneHCID 67166164—
용매Hydrochloric AcidHCID 313—
용매EthanolHCID 702—
용매WaterHCID 962—
용매IsopropanolHCID 3776—
생성물3-(3-Chloro-4-hydroxy-5-methoxy-phenyl)-1-(5-ethyl-4-phenyl-thiophen-2-yl)-propan-1-oneHCID 5924899559.7%

반응 단계

A solution of 1-(5-ethyl-4-phenyl-thiophen-2-yl)-ethanone (200 mg, 0.869 mmol) and 3-chloro-4-hydroxy-5-methoxybenzaldehyde (194 mg, 1.04 mmol) in ethanol (2 mL) and 5 N HCl in isopropanol (1 mL) is stirred at rt for 18 h. The dark green solution is diluted with water and extracted with EA. The organic extract is evaporated, dissolved in methanol (5 mL) and THF (5 mL) and treated with Pd/C (150 mg, 10% Pd). The slurry is hydrogenated under 1.8 bar of H2 for 18 h. The mixture is filtered over celite, the solvent is removed in vacuo and the crude product is purified by CC on silica gel eluting with heptane:EA 7:3 to give 3-(3-chloro-4-hydroxy-5-methoxy-phenyl)-1-(5-ethyl-4-phenyl-thiophen-2-yl)-propan-1-one (208 mg) as a colourless oil; LC-MS: tR=1.10 min, [M+1]+=401.12; 1H NMR (CDCl3): δ 7.58 (s, 1H), 7.46-7.30 (m, 5H), 6.83 (d, J=1.8 Hz, 1H), 6.67 (d, J=1.8 Hz, 1H), 3.88 (s, 3H), 3.16 (t, J=7.6 Hz, 2H), 2.98 (t, J=7.6 Hz, 2H), 2.91 (q, J=7.6 Hz, 2H), 1.30 (t, J=7.6 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951794B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-070df507d40d472e9b1ddeb4041c5f96
출처 메모uspto-grants-2011_05