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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1983891생성일: 2026년 10월 26일

Dichloromethane → 7-Bromo-1-chloronaphthalene

https://huagongshe.com/reaction/1983891

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물7-Bromonaphthalen-2-amineHCID 22240243—
반응물Sodium NitriteHCID 23668193—
촉매Cuprous chlorideHCID 62652—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물7-Bromo-1-chloronaphthaleneHCID 5348567143%

반응 단계

A mixture of the product from Step C (6.0 g, 30 mmol) and 6 M HCl (13.4 ml) was stirred at room temperature until a solid formed. The mixture was cooled to 0° C. and a solution of sodium nitrite (1.9 g, 30 mmol) in water (5.6 ml) was slowly added keeping the temperature below 5° C. The resulting brown slurry was stirred at 0° C. for 15 minutes and then a solution of copper(I) chloride (3.3 g, 30 mmol) in 6 M HCl (15.4 ml) was added. The mixture was stirred at 0° C. for 10 minutes, then warmed to room temperature and stirred at 60° C. for 30 minutes. After cooling to room temperature, dichloromethane was added. The mixture was filtered through diatomaceous earth and the filtrate was extracted with dichloromethane three times. The combined organic layers were washed with water and dried over magnesium sulfate to give 7-bromo-1-chloronaphthalene (2.8 g, 43%) after chromatography (100% hexanes): 1H NMR (300 MHz, DMSO-d6) δ 8.30 (d, J=1.8 Hz, 1H), 7.96-8.02 (m, 2H), 7.74-7.78 (m, 2H), 7.55 (t, J=7.8 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07541357B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-a2b9c6929ecb469d825bfe09f6a4afba
출처 메모uspto-grants-2009_06