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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494417생성일: 2026년 10월 25일

Ethanone, 1-(3,5-bis(phenylmethoxy)phenyl)- → 1-(3,5-Bis(phenylmethoxy)phenyl)-2-bromoethan-1-one

https://huagongshe.com/reaction/494417

반응식

참여 물질

역할이름HCID투입량
반응물Ethanone, 1-(3,5-bis(phenylmethoxy)phenyl)-HCID 120098—
반응물Tetra-n-butylammonium tribromideHCID 23500184—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물1-(3,5-Bis(phenylmethoxy)phenyl)-2-bromoethan-1-oneHCID 120097—

반응 단계

To a stirred solution of 1-[3,5-bis(benzyloxy)phenyl]ethanone (5 g, 15.04 mmol) in tetrahydrofuran (60 mL) and methanol (35 mL) was added tetrabutylammonium tribromide (7.25 g, 15.04 mmol) in tetrahydrofuran (20 mL) at room temperature. The reaction mixture was stirred for 24 hours and the solvent removed in vacuo. The residue was dissolved in ethyl acetate (100 mL) and washed with water (2×50 mL). The combined organic extracts were dried over magnesium sulfate and concentrated to afford the desired compound as a yellow oil in quantitative yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538141B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-37b82bc9545047b0916a4cec67c3ded1
출처 메모uspto-grants-2009_05