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HRID 1361221作成日:2026年10月24日

1-(toluene-4-sulfonyl)-1H-pyrazole-3-carbaldehyde → 1-[1-(toluene-4-sulfonyl)-1H-pyrazol-3-yl]-propan-1-ol

https://huagongshe.com/ja/reaction/1361221

反応式

関与物質

役割名称HCID仕込み量
反応物1-(toluene-4-sulfonyl)-1H-pyrazole-3-carbaldehydeHCID 59278370—
反応物HCID 178461633HCID 178461633—
溶媒TetrahydrofuranHCID 8028—
溶媒Ammonia chlorideHCID 20976574—
生成物1-[1-(toluene-4-sulfonyl)-1H-pyrazol-3-yl]-propan-1-olHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07879873B2
出典データセットuspto-grants-2011_02
ORD IDord-99b443aa4c784028b2f21341c07a545e
出典メモuspto-grants-2011_02