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HRID 507007作成日:2026年10月25日

Allyl bromide → Methyl 3-[allyl(2-bromo-5-methoxybenzoyl)amino]-4-methylbenzoate

https://huagongshe.com/reaction/507007

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物Sodium hydrideHCID 24758—
反応物Methyl 3-[(2-bromo-5-methoxybenzoyl)amino]-4-methylbenzoateHCID 2673200—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 3-[allyl(2-bromo-5-methoxybenzoyl)amino]-4-methylbenzoateHCID 67018574—

反応手順

To a slurry of NaH (680 mg [60% dispersion in oil]) in THF (250 ml) at 0° C. was added methyl 3-[(2-bromo-5-methoxybenzoyl)amino]-4-methylbenzoate (5.36 g) portionwise. The reaction was stirred for 30 minutes at room temperature when allyl bromide (1.6 ml) was added dropwise and the solution was stirred for a further 20 hours at room temperature. The reaction mixture was quenched with water and then concentrated. The residue was dissolved in ethyl acetate and washed with water (×2), brine, dried (magnesium sulfate) and concentrated. The residue was purified by column chromatography on a silica column eluting using a gradient of iso-hexane to 50% ethyl acetate/iso-hexane to yield methyl 3-[allyl(2-bromo-5-methoxybenzoyl)amino]-4-methylbenzoate as a colourless oil (4.88 g); Mass Spectrum: M+H+ 417.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07786115B2
出典データセットuspto-grants-2010_08
ORD IDord-5e296b344d4a4837baebf597892a2bb8
出典メモuspto-grants-2010_08