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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226508생성일: 2026년 10월 23일

3-Bromo-2-methyl-1-propene → 2-(3,5-Bis-benzyloxyphenyl)-4-methyl-pent-4-enoic acid methyl ester

https://huagongshe.com/ko/reaction/226508

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참여 물질

역할이름HCID투입량
반응물3-Bromo-2-methyl-1-propeneHCID 357785—
반응물Methyl [3,5-bis(benzyloxy)phenyl]acetateHCID 640121—
반응물Lithium diisopropylamideHCID 2724682—
반응물Tetrahydrofuran heptane ethylbenzolHCID 22742125—
용매TetrahydrofuranHCID 8028—
생성물2-(3,5-Bis-benzyloxyphenyl)-4-methyl-pent-4-enoic acid methyl esterHCID 5775503994.3%

반응 조건

온도0 °C

반응 단계

A 2M solution of LDA in THF-heptane-ethylbenzene (21.5 mL, 43.0 mmol) was added dropwise over 12 min to a stirred solution of (3,5-bis-benzyloxyphenyl)acetic acid methyl ester (13.0 g, 35.9 mmol) in THF (80 mL) at −78° C. under a nitrogen atmosphere. The temperature was maintained below −70° C. for a further 50 min then 3-bromo-2-methylpropene (4.0 mL, 39.7 mmol) was added in one portion and the reaction mixture was warmed to 0° C. After 2 h the mixture was concentrated in vacuo, diluted with sat. aq. NH4Cl (100 mL) and extracted with EtOAc (100 mL). The organic layer was washed with brine (100 mL), dried (MgSO4), concentrated in vacuo and purified by flash chromatography (silica, 0-10% EtOAc in petroleum ether) to afford the title product as a yellow oil (14.1 g, 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557244B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-e4cd3a373ea64c1397c60db3820a9fa0
출처 메모uspto-grants-2009_07