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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269654Generated: October 25, 2026

Methyl chloroacetate → Methyl 5-isoquinolyloxyacetate

https://huagongshe.com/reaction/2269654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroacetateHCID 7295—
ReactantIsoquinolin-5-olHCID 30386—
ReactantSodium MethoxideHCID 10942334—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-isoquinolyloxyacetateHCID 453435—

Reaction Steps

To an ice-cooled solution of 29.0 g of 5-hydroxyisoquinoline in 300 ml of DMF, 11.0 g of sodium methylate was added portionwise. After stirring for 30 min, 17.9 ml of methyl chloroacetate was added dropwise, and the resultant mixture was stirred at room temperature overnight and concentrated under reduced pressure. To the residue, 300 ml of toluene and 300 ml of water were added, and the whole mixture was filtered. The aqueous layer was extracted with 50 ml of toluene, and the combined toluene solution was treated with 2 g of charcoal and evaporated to give methyl 5-isoquinolyloxyacetate. The ester was dissolved in 100 ml of methanol, reacted with 80 ml of 3 N sodium hydroxide aqueous solution for 30 min. The reaction mixture was concentrated under reduced pressure, diluted with 80 ml of water and 160 ml of acetone, and neutralized with 20 ml of concentrated hydrochloric acid. The precipitates formed were filtered, washed with 80 ml of 50% aqueous acetone, and dried to give 34.5 g (85% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329502B1
Source datasetuspto-grants-2001_12
ORD IDord-6542a141a4e6475aa07e244374ab5fa6
Source noteuspto-grants-2001_12