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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042102Generated: November 1, 2026

1,2-Dimethoxyethane → Ethyl 5-chloro-2-(quinolin-6-yl)benzoate

https://huagongshe.com/reaction/2042102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
ReactantQuinolin-6-ylboronic Acid (contains varying amounts of Anhydride)HCID 4192671—
ReactantEthyl 5-chloro-2-iodobenzoateHCID 51341862—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductEthyl 5-chloro-2-(quinolin-6-yl)benzoateHCID 6725387339.1%

Reaction Steps

A degassed mixture of ethyl 5-chloro-2-iodobenzoate (0.621 g, 2.00 mmol), Pd(PPh3)4 (0.116 mg, 0.1 mmol), quinolin-6-ylboronic acid (0.381 g, 2.2 mmol), K2CO3 (0.553 g, 4.0 mmol), dimethoxyethane (20 mL), and water (5 mL) was heated under reflux overnight. Solvents were removed under reduced pressure. The residue was diluted with sat'd NH4Cl (15 mL) and extracted with EtOAc (3×30 mL). The combined organic layers were dried (MgSO4), concentrated in vacuo and purified by chromatography to afford ethyl 5-chloro-2-(quinolin-6-yl)benzoate (0.244 g, 39% yield) as a colorless oil. MS (ESI) m/z: 312.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586565B2
Source datasetuspto-grants-2013_11
ORD IDord-b5ecbd688b034e24845d8fdbe1d4dd0c
Source noteuspto-grants-2013_11