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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350137Generated: November 1, 2026

Potassium Carbonate → 6-Bromo-5-hydroxy-2-isopropoxy-4-(trifluoromethyl)quinoline

https://huagongshe.com/reaction/1350137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Benzyloxy-6-bromo-2-isopropoxy-4-(trifluoromethyl)quinolineHCID 21094380—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventMethanesulfonic AcidHCID 6395—
Product6-Bromo-5-hydroxy-2-isopropoxy-4-(trifluoromethyl)quinolineHCID 13579778092%

Reaction Steps

A solution of 5-benzyloxy-6-bromo-2-isopropoxy-4-(trifluoromethyl)quinoline (13.5 g, 30.8 mmol) in 31 mL methanesulfonic acid and 31 mL acetic acid was stirred at rt for 10 h, whereupon it was poured in water (500 mL), neutralized with K2CO3 (ca. 75 g) and extracted with EtOAc (3×200 mL). The combined organic layers were washed with brine (200 mL), dried over MgSO4, filtered and concentrated. Flash chromatography (2%–5% EtOAc:hexanes, gradient elution) afforded 9.9 g (92%) of 6-bromo-5-hydroxy-2-isopropoxy-4-(trifluoromethyl)quinoline, a yellow-brown oil. 1H NMR (400 MHz, CDCl3) δ 7.71 (d, 1H, J=9.1), 7.38 (d, 1H, J=9.1), 6.23 (s, 1H), 5.53 (sept, 1H, J=6.2), 1.41 (d, 6H, J=6.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214690B2
Source datasetuspto-grants-2007_05
ORD IDord-2ce50820cd6d4c86a35a36b40bf07541
Source noteuspto-grants-2007_05