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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472789Generated: October 30, 2026

Acetic Acid → Methyl Quinoline-8-Carboxylate

https://huagongshe.com/reaction/472789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium CarbonateHCID 10340—
Reactant8-Quinolinecarboxylic acidHCID 66582—
ReactantTrimethylsilyldiazomethaneHCID 167693—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductMethyl Quinoline-8-CarboxylateHCID 1255453380%

Reaction Steps

A solution of (trimethylsilyl)diazomethane (8.0 mL of a 2.0 M solution in hexanes, 16.0 mmol) was added slowly to a suspension of quinoline-8-carboxylic acid (2.0 g, 11.5 mmol) in toluene (80 mL) and MeOH (12 mL) at 0° C. After 30 min at 0° C., the reaction mixture was warmed to room temperature and stirred for 64 h. Aqueous acetic acid was added and then enough saturated aqueous Na2CO3 was added to bring the pH to 7.5. The layers were separated and the aqueous phase was extracted with EtOAc. The combined organic phase was dried (MgSO4SO4), filtered and concentrated in vacuo. The resulting brown oil was purified on 40 g silica gel (2:1 CH2Cl2/EtOAc) to afford 1.72 g (80%) of methyl quinoline-8-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633220B2
Source datasetuspto-grants-2014_01
ORD IDord-e46c9b6757464243a3b4e34f1729b547
Source noteuspto-grants-2014_01