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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 657982생성일: 2026년 10월 25일

Methyl iodide → 1-Bromo-5-(1,1-dimethoxyethyl)-2-methoxy-3-trifluoromethylbenzene

https://huagongshe.com/reaction/657982

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Trimethyl orthoformateHCID 9005—
반응물Potassium CarbonateHCID 11430—
반응물3'-Bromo-4'-hydroxy-5'-(trifluoromethyl)acetophenoneHCID 58085700—
촉매D-Camphorsulfonic AcidHCID 65617—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
용매Heptane waterHCID 57468513—
생성물1-Bromo-5-(1,1-dimethoxyethyl)-2-methoxy-3-trifluoromethylbenzeneHCID 58085697—

반응 단계

1-(3-Bromo-4-hydroxy-5-trifluoromethylphenyl)ethanone (O4.004; 6.8 g) was dissolved in methanol (50 ml) and admixed successively with DL-10-camphorsulfonic acid (111 mg) and trimethyl orthoformate (8 ml). After stirring at RT for 2 h, DMF (75 ml), potassium carbonate (4.98 g) and then slowly, while cooling with ice, iodomethane (3 ml) were added. After stirring at RT for 4 h, the reaction mixture was left to stand overnight and then admixed with n-heptane/water, and the organic phase was removed. The aqueous phase was extracted by shaking once more with n-heptane, and the combined organic phases were then dried over magnesium sulfate, filtered and concentrated. 7 g of the title compound were obtained in sufficient purity.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076336B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-5992c9e592904eba8876e241466c6e2e
출처 메모uspto-grants-2011_12