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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 267083생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/267083

반응식

참여 물질

역할이름HCID투입량
반응물Potassium bisulfateHCID 516920—
반응물Aluminium lithium hydrideHCID 21226445—
반응물N-Methoxy-N-methyl-1-(2-naphthylmethyl)-1H-imidazol-5-ylacetamideHCID 86751125—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-(2-Naphthylmethyl)-1H-imidazol-5-ylacetaldehydeHCID 86751126—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05652257
출처 데이터셋uspto-grants-1997_07
ORD IDord-c40edfa1df2e4e099f9e647045e9a01b
출처 메모uspto-grants-1997_07