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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890912Generated: October 31, 2026

Glycerol → 6-Bromo-7-methylquinoline

https://huagongshe.com/reaction/1890912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycerolHCID 753—
ReactantSulfuric AcidHCID 1118—
ReactantNitrobenzeneHCID 7416—
Reactant4-Bromo-3-methylanilineHCID 23359—
Product6-Bromo-7-methylquinolineHCID 5791101831.4%

Reaction Steps

A mixture of 4-bromo-3-methylaniline (20 g, 107.5 mmol), ferric sulfate (6.6 g, 43.4 mmol), glycerol (40.8 g, 440 mmol), nitrobenzene (8.12 g, 66 mmol), and concentrated sulfuric acid (23 ml) was heated gently. After the first vigorous reaction, the mixture was boiled for 3 h and then evaporated to remove the excess nitrobenzene. The solution was added a saturated aqueous solution of sodium bicarbonate until pH=7-8, then the solution was filtered and extracted with dichloromethane. The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo. The solid was purified by flash column chromatography to give a yellow solid, which was further washed with petroleum ether to give 7.5 g of 6-bromo-7-methyl-quinoline (31% yield): 1H NMR (CDCl3): 2.60 (s, 3H), 7.36 (m, 1H), 7.96 (s, 1H), 8.04 (m, 2H), 8.89 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507489B2
Source datasetuspto-grants-2013_08
ORD IDord-7ca93d444f154be68f99246e895e0e59
Source noteuspto-grants-2013_08