関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Allyl bromide | HCID 7841 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Methyl 3-[(2-bromo-5-methoxybenzoyl)amino]-4-methylbenzoate | HCID 2673200 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Methyl 3-[allyl(2-bromo-5-methoxybenzoyl)amino]-4-methylbenzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07786115B2 |
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| 出典データセット | uspto-grants-2010_08 |
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| ORD ID | ord-5e296b344d4a4837baebf597892a2bb8 |
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| 出典メモ | uspto-grants-2010_08 |
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