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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5674생성일: 2026년 10월 23일

Water → 4-[(2-Ethyl-5,6,7,8-tetrahydroquinolin-4-yl)oxymethyl]phenylboronic acid

https://huagongshe.com/ko/reaction/5674

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물4-(Bromomethyl)phenylboronic acidHCID 2735593—
반응물2-Ethyl-5,6,7,8-tetrahydroquinolin-4(1H)-oneHCID 14950475—
용매DimethylformamideHCID 6228—
생성물4-[(2-Ethyl-5,6,7,8-tetrahydroquinolin-4-yl)oxymethyl]phenylboronic acidHCID 1517142299.3%

반응 단계

Sodium hydride (60% dispersion in oil; 180 mg) was added to a mixture of 2-ethyl-5,6,7,8-tetrahydro-4(1H)-quinolone (660 mg) and 4-bromomethylphenylboronic acid (800 mg) (obtained as described in J. Amer. Chem. Soc. 1958, 80, 835) in DMF (12 ml) under an atmosphere of argon. The mixture was stirred for 40 hours and then water (0.2 ml) was added. Volatile material was removed by evaporation and the residue was dissolved in warm 0.5M sodium hydroxide solution (10 ml). Insoluble material was removed by filtration and the filtrate was acidified to pH 4 with 20% citric acid solution. The precipitate solid was collected by filtration, washed with water (20 ml) and dried under high vacuum to give 4-[(2-ethyl-5,6,7,8-tetrahydroquinolin-4-yl)oxymethyl]phenylboronic acid (C) (1.15 g), m.p. 229°-231° C.; NMR (d6 -DMSO): 1.3(t,3H), 1.6-1.9(m,4H), 2.5-2.7(m,2H), 2.75-2.95(m, 4H), 5.4(s,2H), 7.3(d,2H), 7.4(s,1H, 7.5(d,2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245035
출처 데이터셋uspto-grants-1993_09
ORD IDord-453bbeae00f848f6ad982371dbf56ba9
출처 메모uspto-grants-1993_09