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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827947Generated: November 1, 2026

Methyl chloroformate → 6-Methoxy-2-(3-methoxyphenyl)quinoline

https://huagongshe.com/reaction/1827947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
Reactant6-Methoxyquinoline N-oxideHCID 253821—
ReactantHCID 178490745HCID 178490745—
SolventTetrahydrofuranHCID 8028—
Product6-Methoxy-2-(3-methoxyphenyl)quinolineHCID 2206461046.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-methoxyquinoline-N-oxide (175 mg, 1.0 mmol) in THF (3 mL) at room temperature is added methyl chloroformate (77 uL, 1.0 mmol). The mixture is cooled to 0° C. and 3-methoxyphenylmagnesium bromide (2 mL of 1M, 2 mmol) is added dropwise. The mixture is stirred for 16 h while warming to room temperature. The solvent is removed in vacuo and the resulting residue is partitioned between water and CH2Cl2. The organic phase is washed with water and brine, dried over MgSO4, filtered and concentrated. Flash chromotography (0–20% EtOAc/hexanes) yields 6-methoxy-2-(3-methoxy-phenyl)-quinoline (123 mg, 46% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056931B2
Source datasetuspto-grants-2006_06
ORD IDord-8c25b71552ab4600b5e5ddfe561eb5d8
Source noteuspto-grants-2006_06