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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711682Generated: October 27, 2026

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

https://huagongshe.com/reaction/1711682

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 numberUS07790756B2
Source datasetuspto-grants-2010_09
ORD IDord-cd8ff515f9ee4738a323a883ab234c98
Source noteuspto-grants-2010_09