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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 260315생성일: 2026년 10월 26일

Sodium hydride → t-Butyl 3-nitrobenzyloxyacetate

https://huagongshe.com/reaction/260315

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-Nitrobenzyl alcoholHCID 69267—
반응물tert-Butyl bromoacetateHCID 79177—
용매DimethylformamideHCID 6228—
생성물t-Butyl 3-nitrobenzyloxyacetateHCID 2240115988%

반응 단계

3-Nitrobenzyl alcohol (5 g, 32.6 mM) was dissolved in DMF (200 ml) and cooled to 5°. Sodium hydride (60% in oil, 1.57 g, 39.2 mM) was added to the stirred solution in portions over 30 minutes, and the mixture cooled to -20°. t-Butyl bromoacetate (5.27 ml, 32.6 mM) was run in dropwise, and the mixture allowed to warm to ambient temperature overnight. Solvent was evaporated, the residue treated with water, and organics extracted into ethyl acetate. The combined organic layers were washed with water and brine, and dried over MgSO4. Crude product was purified by chromatography on silica, eluting with a gradient from hexane/dichloromethane (95:5) to dichloromethane, to give t-butyl 3-nitrobenzyloxyacetate (7.71 g, 88%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05527791
출처 데이터셋uspto-grants-1996_06
ORD IDord-acea8aa7dfb041c3bd43bcaaea3b9530
출처 메모uspto-grants-1996_06