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HRID 226508作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物3-Bromo-2-methyl-1-propeneHCID 357785—
反応物Methyl [3,5-bis(benzyloxy)phenyl]acetateHCID 640121—
反応物Lithium diisopropylamideHCID 2724682—
反応物Tetrahydrofuran heptane ethylbenzolHCID 22742125—
溶媒TetrahydrofuranHCID 8028—
生成物2-(3,5-Bis-benzyloxyphenyl)-4-methyl-pent-4-enoic acid methyl esterHCID 5775503994.3%

反応条件

温度0 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557244B2
出典データセットuspto-grants-2009_07
ORD IDord-e4cd3a373ea64c1397c60db3820a9fa0
出典メモuspto-grants-2009_07