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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5674Generated: October 26, 2026

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

https://huagongshe.com/reaction/5674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(Bromomethyl)phenylboronic acidHCID 2735593—
Reactant2-Ethyl-5,6,7,8-tetrahydroquinolin-4(1H)-oneHCID 14950475—
SolventDimethylformamideHCID 6228—
Product4-[(2-Ethyl-5,6,7,8-tetrahydroquinolin-4-yl)oxymethyl]phenylboronic acidHCID 1517142299.3%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245035
Source datasetuspto-grants-1993_09
ORD IDord-453bbeae00f848f6ad982371dbf56ba9
Source noteuspto-grants-1993_09