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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 742525생성일: 2026년 10월 23일

Water → Methyl 2-butenyloxy-4-octyloxybenzoate

https://huagongshe.com/ko/reaction/742525

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물1-Bromobut-1-eneHCID 35945—
반응물Methyl 2-hydroxy-4-octyloxybenzoateHCID 11536459—
용매Methyl Ethyl KetoneHCID 6569—
생성물Methyl 2-butenyloxy-4-octyloxybenzoateHCID 6773832889.9%

반응 단계

To a solution of 22.0 g (78.5 mmol) of the compound (29) and 65.0 g (471 retool) of potassium carbonate mixed in 300 ml of 2-butanone were added 32.0 g (236 mmol) of butenyl bromide and the whole was refluxed for 18 hours. Water was added to the solution and the whole was extracted with ethyl acetate. After removal of the solvent by distillation, the residue was purified by silica gel column chromatography to obtain 23.6 g of methyl 2-butenyloxy-4-octyloxybenzoate as a colorless clear liquid (yield: 89.9%). Then, 20.0 g (59.8 mmol) of the resulting compound was dissolved in 100 ml of methanol. The solution was poured into a solution of 12.0 g (300 mmol) of sodium hydroxide dissolved in 40 ml of water and 400 ml of methanol. The whole was refluxed for another 2 hours. After removal of the solvent by distillation, the resulting white solid was dissolved in water and the solution was rendered acidic by adding hydrochloric acid, whereby white precipitate formed. The precipitate was extracted with methylene chloride. After removal of the solvent by distillation, the residue was purified by silica gel column chromatography to obtain 15.3 g of 2-butenyloxy-4-octyloxybenzoic acid (30) (yield: 80.0%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05554706
출처 데이터셋uspto-grants-1996_09
ORD IDord-3e707464077b474bb8d7e5c0ecfe2d46
출처 메모uspto-grants-1996_09