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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881044Generated: October 31, 2026

Glycerol → Methyl 6-quinolineacetate

https://huagongshe.com/reaction/881044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycerolHCID 753—
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant4-Aminophenylacetic acidHCID 14533—
ReactantSodium HydroxideHCID 14798—
CatalystIodineHCID 807—
ProductMethyl 6-quinolineacetateHCID 1514202—

Reaction Conditions

Temperature140 °C

Reaction Steps

Sulphuric acid (67.5 ml) was added to 4-Aminophenylacetic acid (45 g, 297 mmol), glycerol (61.7 g, 67 mmol), and iodine (1.14 g, 4 mmol) drop-wise at rt. The mixture was heated to 140° C. for 24 h. After that reaction mixture cooled to rt and pH adjusted to 5 using 10% sodium hydroxide solution. To this methanol (350 ml) and sulphuric acid (3 ml) was added and heated to 100° C. for 24 h. Reaction mixture filtered through celite and filtrate was evaporated on rotavapour to obtain the residue. pH of the residue was adjusted to 5 using 4% NaOH solution and extracted with EtOAc. EtOAc layer was dried on anhydrous Na2SO4 and EtOAc removed on rotavapour to obtain the crude. Crude was purified by column using EtOAc and Petether as eluent to obtain methyl-2-(quinolin-6-yl)acetate (11.2 g). Methyl-2-(quinolin-6-yl)acetate (11.2 g) was dissolved in Methanol (8 ml) and water (8 ml) and added sodium hydroxide (3.3 g, 82 mmol). This mixture stirred for 30 mins and methanol removed on rotavapour to obtain the residue. Residue was acidified to pH 5 using 0.8 N HCl to obtain the solid. Solid was filtered and dried to obtain the title compound (8.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993612B2
Source datasetuspto-grants-2015_03
ORD IDord-5c3777c02e66404595ddc32402756255
Source noteuspto-grants-2015_03