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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1954048생성일: 2026년 10월 27일

Hydrochloric Acid → 1,2-Bis(3,4-dimethoxyphenyl)ethanone

https://huagongshe.com/reaction/1954048

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물VeratroleHCID 7043—
반응물(3,4-Dimethoxyphenyl)acetyl chlorideHCID 3604458—
반응물Aluminum(III) ChlorideHCID 6451240—
생성물1,2-Bis(3,4-dimethoxyphenyl)ethanoneHCID 23111198%

반응 단계

Powdered anhydrous aluminum chloride (0.78 g) was slowly added to a stirred mixture of 1,2-dimethoxybenzene (0.64 g, 4.66 mmol) and 3,4-dimethoxyphenylacetyl chloride (1.0 g, 4.66 mmol) in 10 mL freshly distilled dry dichloromethane. An exothermic reaction occurred. The orange solution became brown as the mixture refluxed. The reaction mixture was heated to reflux for an additional 2 h and then allowed to cool to room temperature. The cooled solution was poured into a mixture containing of 5 g crushed ice and 5.5 mL 7.5 N HCl. The organic phase was separated and the aqueous phase was extracted three times with 10 mL dichloromethane. The combined dichloromethane extract was dried (Na2SO4), filtered, and evaporated to give a white solid, which was crystallized from ethanol to give pure white needles of 11a in 98% yield; mp 105-107° C. (lit.30 mp 104-106° C.); 1H NMR δ 3.85 (s, 6H), 3.91 (s, 3H), 3.94 (s, 3H), 4.18 (s, 2H), 6.81 (m, 2H), 6.91 (m, 2H), 7.56 (d, 1H, J=2.0), 7.66 (dd, 1H, J=8.4,2.0); 13C NMR δ 45.2, 56.3, 56.4, 56.5, 110.4, 111.1, 111.8, 112.8, 121.3, 121.9, 123.9, 127.9, 130.2, 148.4, 149.5, 153.8, 197.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06121275
출처 데이터셋uspto-grants-2000_09
ORD IDord-0055ae4d18f74f75912e8ca592f59415
출처 메모uspto-grants-2000_09