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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51575생성일: 2026년 10월 23일

Reserpine → 4-Bromo-2-chloro-1-phenoxybenzene

https://huagongshe.com/ko/reaction/51575

반응식

참여 물질

역할이름HCID투입량
반응물ReserpineHCID 5770—
반응물TriethylamineHCID 8471—
반응물4-Bromo-2-chlorophenolHCID 19859—
반응물Phenylboronic AcidHCID 66827—
촉매Cupric acetateHCID 8895—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
용매HeptaneHCID 8900—
생성물4-Bromo-2-chloro-1-phenoxybenzeneHCID 22736309—

반응 단계

A mixture of 4-bromo-2-chlorophenol (2.07 g, 10 mmol), phenyl boronic acid (3.66 g, 30 mmol), copper(II) acetate (2.0 g, 1.1 mmol) and 4A powdered molecular sieves (20 g) in dichloromethane (100 mL) was treated with triethylamine (5.0 g, 50 mmol) then stirred at ambient temperature for 5 days. The mixture was diluted with heptane (100 mL), then filtered through a bed of celite. The filtrate was concentrated under reduced pressure to remove dichloromethane. The mixture was extracted with IN hydrochloric acid, 15 wt % aqueous sodium hydroxide, brine and then dried over magnesium sulfate. The mixture was filtered and the filtrate concentrated under reduced pressure to provide (1.27 g, 45%): 1H NMR (DMSO-d6, 400 MHz) δ 7.87(s, 1H), 7.55(d, 1H), 7.40(t, 2H), 7.17(t, 1H), 6.99(m, 3H); MS MH+283; RP-HPLC (Hypersil HS, 5 μm, 100 A 4.6×250 mm; 25%-100% acetonitrile—0.05 M ammonium acetate over 10 min, 1 m/min) tr 14.42min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713474B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-11c4d1aba29d43eb826cea2fa995c699
출처 메모uspto-grants-2004_03