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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981921Generated: October 30, 2026

Ethyl bromoacetate → Ethyl[(9-amino-1,2,3,4-tetrahydroacridin-8-yl)oxy]acetate

https://huagongshe.com/reaction/981921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 136404540HCID 136404540—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl[(9-amino-1,2,3,4-tetrahydroacridin-8-yl)oxy]acetateHCID 2006860772.91%

Reaction Steps

8-Hydroxy-1,2,3,4-tetrahydro-9-acridinamine hydrochloride (18.07 g) was suspended in 500 ml of dry dimethylformamide. Potassium carbonate (22.6 g) was added, and the reaction mixture was stirred vigorously for 30 mins. Ethyl bromoacetate (18.0 g) was added dropwise, and the reaction was stirred vigorously overnight. The reaction mixture was distributed between ethyl acetate and water, and the organic layer was separated. The aqueous phase was extracted three times with ethyl acetate, and the combined organic phase was washed with water, dried, filtered, and the filtrate evaporate. The residue was purified by flash chromatography (ethyl acetate, then 5% triethylamine/ethyl acetate) to give 15.75 g (72.91%) of product, mp 141°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994452
Source datasetuspto-grants-1991_02
ORD IDord-61a0c16f2c874c5eb86c97a86e18353c
Source noteuspto-grants-1991_02