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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25002생성일: 2026년 10월 23일

Sodium hydride → Ethyl 3-((4-(2-fluorobenzyloxy)phenyl)-methylthio)propionate

https://huagongshe.com/ko/reaction/25002

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물alpha-Bromo-o-fluorotolueneHCID 67968—
반응물Ethyl 3-((4-hydroxyphenyl)-methylthio)propionateHCID 21964457—
반응물HCID 178418361HCID 178418361—
용매DimethylformamideHCID 6228—
생성물Ethyl 3-((4-(2-fluorobenzyloxy)phenyl)-methylthio)propionateHCID 21964542—

반응 단계

To a solution of NaH (60% dispersed in oil, 0.054 g, 1.3 mmol) in dry DMF (10 ml) was added Ethyl 3-((4-hydroxyphenyl)-methylthio)propionate (Step B, 2.5 g, 1.0 mmol). When the evolution of hydrogen ceased, 2-Fluorobenzyl bromide (0.263 g, 1.3 mmol) was added. The reaction mixture was stirred for 4 hours at room temperature, quenched with sat. NH4Cl, and concentrated in vacuo. The crude residue was taken in EtOAc and washed twice with water and brine. The aqueous layer was washed one more time with EtOAc. The combined organic layers were dried over Na2SO4, filtered and concentrated. The purification was done by flash chromatography on silica gel column (hex: ethyl acetate, 4:1) to provide the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858602B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-bef4aa0a002b41ddad0dd66ab634e9b6
출처 메모uspto-grants-2005_02