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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 330263생성일: 2026년 10월 24일

Benzyl Bromide → 2-(2-Naphthalenyl)-3-phenylpropionitrile

https://huagongshe.com/ko/reaction/330263

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Sodium hydrideHCID 24758—
반응물2-NaphthylacetonitrileHCID 82008—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-(2-Naphthalenyl)-3-phenylpropionitrileHCID 1496063640%

반응 단계

To a refluxing solution of NaH (3.00 g, 75 mmol, 60% dispersion) in DME (150 mL) was added a solution of 2-naphthaleneacetonitrile (12.5 g, 75 mmol) and benzyl bromide (12.8 g, 75 mmol) in DME (75 mL) dropwise over 50 minutes. The resulting solution was kept at reflux for 3 hours and then cooled to room temperature. The volatiles were removed in vacuo and the residue was partitioned between Et2O (100 mL) and H2O (100 mL). The aqueous phase was washed with Et2O (1×150 mL), the organics were dried (MgSO4) and concentrated in vacuo. This residue was purified by preparative HPLC (SiO2 : gradient hexane/EtOAc) to give the title compound as a white solid (7.71 g, 40%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04895861
출처 데이터셋uspto-grants-1990_01
ORD IDord-d15056049a82458a98917c13f3a87301
출처 메모uspto-grants-1990_01