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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2361835생성일: 2026년 10월 26일

Methanol → HCID 71149847, 화합물

https://huagongshe.com/reaction/2361835

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참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물4-(4'-Chlorobenzyl)pyridineHCID 78124—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물N-BOC-N,N-Bis(2-chloroethyl)amineHCID 11230235—
용매TolueneHCID 1140—
생성물HCID 71149847HCID 711498470.7%

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온도0 °C

반응 단계

Under nitrogen, a solution of bis-(2-chloro-ethyl)-carbamic acid tert-butyl ester* (1.54 g, 6.36 mmol) in toluene (10 mL) was cooled in ice. 4-(4-Chloro-benzyl)-pyridine (1.30 g, 6.36 mmol) was added, followed over two minutes by sodium hexamethyldisilazide solution (10 mL, 20 mmol, 2M in THF). The mixture was stirred at 0° C. for 3.5 hours then allowed to warm to room temperature and stirred for a further 20 hours. Methanol was added then the mixture was concentrated in vacuo. The residue was taken up in ethyl acetate and washed with 1N hydrochloric acid (×3) and brine, dried (MgSO4), filtered and concentrated to afford a residue which was purified by column chromatography (SiO2), eluting with gradient of 2M methanolic ammonia in dichloromethane (1% to 5%). A second purification by column chromatography (SiO2), eluting with 50% ethyl acetate/petrol gave the title compound (16 mg, 0.7%). LCMS (PS-A2) Rt 2.65 min [M+H]+ 373. *This starting material can be made by the method described in J. Chem. Soc., Perkin Trans 1, 2000, p3444-3450

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08691806B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-5400f2c7e01743888eaeed9cb6b75908
출처 메모uspto-grants-2014_04