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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900398Generated: October 30, 2026

Methylparaben → Methyl 4-[(quinolin-4-yl)methoxy]benzoate

https://huagongshe.com/reaction/900398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylparabenHCID 7456—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactant4-(Chloromethyl)quinolineHCID 12355701—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
ProductMethyl 4-[(quinolin-4-yl)methoxy]benzoateHCID 53689041—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (430 mg, 60%, 10.75 mmol) was placed in a flask with hexane and stirred under nitrogen. After 10 minutes the hexane was discarded and 10 ml dry DMF was added. After cooling to 0° C., 4-hydroxy-benzoic acid methyl ester Q-2 (1.67 g, 11 mmol) was added and the mixture stirred for 15 minutes. 4-Chloromethyl-quinoline Q-1 (1.8 g, 10.1 mmol) was dissolved in 3 mL of DMF and added dropwise to the reaction mixture. The temperature was raised to 130° C. and the mixture stirred for a half hour. After cooling to room temperature the reaction mixture was poured into 50 mL 1N sodium hydroxide solution and extracted three times with 20 mL dichloromethane. The combined organic layers were washed twice with water, dried over sodium sulfate and concentrated in vacuo. The crude product (2.5 g) was recrystallized from ethyl ether to give 4-(quinolin-4-ylmethoxy)-benzoic acid methyl ester (1.6 g, 5.45 mM) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358373B2
Source datasetuspto-grants-2008_04
ORD IDord-ca819de813ae4c0681792a79e9720bd9
Source noteuspto-grants-2008_04