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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 361967생성일: 2026년 10월 26일

Acetic Acid → 2,6-Dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenone

https://huagongshe.com/reaction/361967

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrogen BromideHCID 260—
반응물2,6-Dichloro-2',3',4'-trimethoxy-6'-methyl-benzophenoneHCID 22719953—
용매WaterHCID 962—
생성물2,6-Dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenoneHCID 54569551—

반응 조건

온도75 °C

반응 단계

A mixture of 2,6-dichloro-2',3',4'-trimethoxy-6'-methyl-benzophenone (1.78 g; 5 mmol) hydrobromic acid (7.5 ml; 30% in acetic acid) and acetic acid (7.5 ml) is stirred at 75° C. for 2 hours. Water is added and the mixture extracted with methylenechloride. The extract is washed with waterand shaken with 2N sodium hydroxide. The alcaline solution is acidified with hydrochloric acid, the separated compound dissolved in methylenechloride and the solution washed with water. After evaporation ofthe solvent purification is carried out by chromatography (flash column, filled with 36 g of silicagel; elution with 500 ml of petrolether/ethylacetate (4:1; v/v) and 250 ml of petrolether/ethylacetate(1:1; v/v)). the fraction containing the compound is concentrated, the compound crystallized. The yellow crystals are washed with petrolether andsucked off; 0.64 g (39% y), mp. 182° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05866722
출처 데이터셋uspto-grants-1999_02
ORD IDord-f2bc4d1e56aa4859abea606d965acb6e
출처 메모uspto-grants-1999_02