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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339061Generated: October 26, 2026

Methyl iodide → (R)-7-(2-methoxypropoxy)-2-methylquinoline

https://huagongshe.com/reaction/339061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(R)-1-(2-methylquinolin-7-yloxy)propan-2-olHCID 70983350—
SolventDimethylformamideHCID 6228—
Product(R)-7-(2-methoxypropoxy)-2-methylquinolineHCID 7098332851%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of NaH (60% dispersion in oil, 95 mg, 2.4 mmol) in DMF (8 mL) was added dropwise a solution of (R)-1-(2-methylquinolin-7-yloxy)propan-2-ol (344 mg, 1.58 mmol) in DMF (4 mL) at 0° C. under nitrogen. The reaction mixture was stirred at 0° C. for 30 minutes. MeI (0.198 mL, 3.17 mmol) was added dropwise. The reaction was stirred at ambient temperature overnight. The reaction mixture was partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc. The combined organic layers were washed with water and brine, dried and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (5:1 hexanes/EtOAc) to give (R)-7-(2-methoxypropoxy)-2-methylquinoline (185 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-a8613c79550f4d7faa34c4278664d870
Source noteuspto-grants-2014_11