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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532841Generated: October 29, 2026

Glycerol → 7-Methoxy-6-methylquinoline

https://huagongshe.com/reaction/532841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycerolHCID 753—
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium HydroxideHCID 14798—
Reactant3-Methoxy-4-methylanilineHCID 27882—
ReactantSodium 3-nitrobenzenesulfonateHCID 31389—
Solvent1,4-DioxaneHCID 31275—
Product7-Methoxy-6-methylquinolineHCID 5936616598.2%

Reaction Conditions

Temperature150 °C

Reaction Steps

Using a minimal amount of dioxane, 3-methoxy-4-methylaniline (5.00 g, 36.5 mmol) was slowly added to a mixture of sodium m-nitrobenzenesulfonate (6.62 g, 29.4 mmol), MsOH (20 mL), and FeSO4.7H2O (0.39 g, 1.4 mmol) in a 100 mL round bottom flask heated to an internal temperature of 145-155° C. Glycerol (10.75 g, 116.8 mmol) was then added dropwise via addition funnel while keeping the internal temperature at 145-155° C. After addition, the reaction was stirred in a 150° C. oil bath until LCMS indicated completion (4-6 h). After being cooled to rt, ice (20 g) was added, then the solution was neutralized with 10 N NaOH (calculated to same eq of MsOH) at a speed to keep the internal temperature below 40° C. A thick suspension appeared after addition, and this was extracted with EtOAc (50 mL×3). The organic layer was filtered through a Celite pad to remove insoluble black particles and then purified by flash column chromatography on silica gel to give the desired product (5.0 g, 79%). MS (ES) m/z 174.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853202B2
Source datasetuspto-grants-2014_10
ORD IDord-643705ef8a114d9d916aff19b4da72f6
Source noteuspto-grants-2014_10