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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2088984생성일: 2026년 10월 26일

Azobisisobutyronitrile → 2-(Bromomethyl)-6-fluoronaphthalene

https://huagongshe.com/reaction/2088984

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물BromineHCID 24408—
반응물N-bromobutanimideHCID 67184—
반응물2-Fluoro-6-methylnaphthaleneHCID 2727845—
용매Carbon TetrachlorideHCID 5943—
생성물2-(Bromomethyl)-6-fluoronaphthaleneHCID 594633—

반응 조건

온도70 °C

반응 단계

To a solution of 2-fluoro-6-methylnaphthalene (0.750 g, 4.68 mmol) in carbon tetrachloride (20 mL) was added NBS (0.917 g, 5.15 mmol) and bromine (0.265 mL, 5.15 mmol) followed by AIBN (0.077 g, 0.47 mmol). The reaction mixture was heated to 70° C. and allowed to stir for 4 hours. It was then cooled to room temperature, partitioned between water and EtOAc, and the aqueous layer was extracted three times with EtOAc. The combined organic layers were dried over sodium sulfate, filtered, concentrated in vacuo and subjected to silica gel chromatography eluting with 5-50% EtOAc in hexanes to yield 2-(bromomethyl)-6-fluoronaphthalene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08436016B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-b365ea986416468aa8a4aa4724bbbe8a
출처 메모uspto-grants-2013_05