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1-(toluene-4-sulfonyl)-1H-pyrazole-3-carbaldehyde → 1-[1-(toluene-4-sulfonyl)-1H-pyrazol-3-yl]-propan-1-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(toluene-4-sulfonyl)-1H-pyrazole-3-carbaldehyde | HCID 59278370 | — |
| 反応物 | HCID 178461633 | HCID 178461633 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ammonia chloride | HCID 20976574 | — |
| 生成物 | 1-[1-(toluene-4-sulfonyl)-1H-pyrazol-3-yl]-propan-1-ol | HCID 59278348 | — |
反応手順
To a chilled (−40° C.) solution of 1-(toluene-4-sulfonyl)-1H-pyrazole-3-carbaldehyde (1.50 g, 5.99 mmol) in THF was added a 2 M solution of ethylmagnesium chloride (3.00 mL, 6.00 mmol) in THF. After 3 hours, the mixture was diluted with saturated aqueous ammonia chloride and extracted with EtOAc. The combined organic layers were washed with brine, dried over sodium sulfate and the concentrated in vacuo. The residue was purified by reversed-phase HPLC. The major fractions were combined and the solvent was concentrated in vacuo to afford 1-[1-(toluene-4-sulfonyl)-1H-pyrazol-3-yl]-propan-1-ol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07879873B2 |
| 出典データセット | uspto-grants-2011_02 |
| ORD ID | ord-99b443aa4c784028b2f21341c07a545e |
| 出典メモ | uspto-grants-2011_02 |