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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 277976생성일: 2026년 10월 24일

Benzyl Bromide → Benzyl 2-(3-methoxymethoxycarbonylnaphthalen-2-yl)benzoate

https://huagongshe.com/ko/reaction/277976

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물2-(3-(Methoxymethoxycarbonyl)naphthalen-2-yl)benzoic acidHCID 17809303—
반응물Methoxymethyl 2-trifluoromethylsulfonyloxy-3-naphthalenecarboxylateHCID 22626196—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Benzyl 2-(3-methoxymethoxycarbonylnaphthalen-2-yl)benzoateHCID 22626517—

반응 단계

Benzyl bromide (160 μl) and potassium carbonate (202 mg) were added to a solution of 2-(3-(methoxymethoxycarbonyl)naphthalen-2-yl)benzoic acid (410 mg) which was prepared by the same procedure as a series of reaction of Reference Example 4→Reference Example 5 using methoxymethyl 2-trifluoromethylsulfonyloxy-3-naphthalenecarboxylate, in dimethylformamid (5 ml). The mixture was stirred for 22 hours at room temperature. Water was added to the reaction mixture, and the solution was extracted with ethyl acetate. The extract was washed with water and a saturated aqueous solution of sodium chloride, successively, dried over anhydrous sodium sulfate and concentrated. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=8:2) to give the title compound (498 mg) having the following physical data.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06358960B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-fb38f4e051b74180a1a2d7e593c54025
출처 메모uspto-grants-2002_03