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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 249724생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/249724

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 (6.8 g) was dissolved in absolute methanol (50 ml) and treated successively with DL-10-camphorsulfonic acid (111 mg) and trimethyl orthoformate (8 ml). After stirring at RT for 2 h, DMF (75 ml) and potassium carbonate (5.0 g) were added, followed by iodomethane (3 ml). After stirring for 6 h, the batch was allowed to stand overnight and was treated with a 1:1 mixture of n-heptane/water. After separating off the organic phase, it was additionally extracted once with n-heptane and then the combined heptane phases were dried over magnesium sulfate, filtered and concentrated. 7 g of the desired product were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863269B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-d7babac152f64052b75fdb5119acece3
출처 메모uspto-grants-2011_01