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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1950628생성일: 2026년 10월 27일

(4-(Benzyloxy)phenyl)methanol → 4-Benzyloxybenzylamine

https://huagongshe.com/reaction/1950628

반응식

참여 물질

역할이름HCID투입량
반응물(4-(Benzyloxy)phenyl)methanolHCID 70043—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물P,P-Diphenylphosphinic azideHCID 199401—
용매TolueneHCID 1140—
생성물4-BenzyloxybenzylamineHCID 429284581%

반응 단계

To a solution of 4-benzyloxybenzyl alcohol (3.1 g) in toluene (40 ml) were sequentially added diphenylphosphoryl azide (4.8 g) and 1,8-diazabicyclo[5.4.0]undec-7-ene (2.6 g), and the solution was stirred for 25 hours at room temperature. The solution was extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. Obtained by purifying the residue by silica gel column chromatography (hexane-ethyl acetate system), to a solution of the resulting 1-azidomethyl-4-benzyloxybenzene (3.0 g) in tetrahydrofuran (40 ml) were sequentially added water (3 ml) and triethylphosphine (2.0 ml), and the solution was stirred for 1 hour and 10 minutes at room temperature. The reaction solution was concentrated in vacuo, extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (2.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399520B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-48e69354d10f44be8e082ccc009f4604
출처 메모uspto-grants-2013_03