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Sodium hydride → 4-Methyl-3-triisopropylsilanylsulfanyl-benzoic acid ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Tris(propan-2-yl)silanethiol | HCID 3435097 | — |
| 反応物 | Ethyl 3-bromo-4-methylbenzoate | HCID 14945865 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-Methyl-3-triisopropylsilanylsulfanyl-benzoic acid ethyl ester | HCID 66764810 | — |
反応手順
To a 0° C. stirred solution of triisopropylsilanethiol (14.28 mmol, 3.07 mL) in THF was added sodium hydride (14.28 mmol, 0.57 g of a 60 wt % dispersion in mineral oil). After 30 min, the mixture was added to a solution of ethyl 3-bromo-4-methylbenzoate (10.99 mmol, 2.67 g) at room temperature, followed by tetrakis(triphenylphosphine)palladium(0) (0.55 mmol, 0.64 g). The resulting mixture was warmed to reflux and stirred for 18 hours, then cooled to room temperature and subjected to standard aqueous workup to afford the title compound which was used crude in the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09000025B2 |
| 出典データセット | uspto-grants-2015_04 |
| ORD ID | ord-75ea47a9512449939a7d3f0375b27f6f |
| 出典メモ | uspto-grants-2015_04 |