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HRID 267083作成日:2026年10月27日

Potassium bisulfate → 1-(2-Naphthylmethyl)-1H-imidazol-5-ylacetaldehyde

https://huagongshe.com/reaction/267083

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium bisulfateHCID 516920—
反応物Aluminium lithium hydrideHCID 21226445—
反応物N-Methoxy-N-methyl-1-(2-naphthylmethyl)-1H-imidazol-5-ylacetamideHCID 86751125—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2-Naphthylmethyl)-1H-imidazol-5-ylacetaldehydeHCID 86751126—

反応手順

To a suspension of lithium aluminum hydride (40.8 mg, 1.07 mmol) in tetrahydrofuran (5 ml) at -45° C. was added a solution of N-methoxy-N-methyl-1-(2-naphthylmethyl)-1H-imidazol-5-ylacetamide (243 mg, 0.895 mmol) in tetrahydrofuran (5 ml) via cannula at such a rate to maintain the temperature at <-35° C. After the addition was complete, the reaction was allowed to warm to +5° C. and then recooled to -35° C. To this solution was added a solution of potassium bisulfate (272 mg) in water (1 ml). The mixture was stirred for 30 min at room temperature and then filtered through celite. The celite pad was washed with ethyl acetate (25 ml). The combined filtrates were washed with sat. sodium bicarbonate (10 ml) and then water (10 ml). The organic layer was dried (MgSO4), filtered and evaporated in vacuo to give 30 as a clear oil. This material was used as is in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05652257
出典データセットuspto-grants-1997_07
ORD IDord-c40edfa1df2e4e099f9e647045e9a01b
出典メモuspto-grants-1997_07