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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195752Generated: October 30, 2026

2-Bromoethanol → HCID 54258687, compound

https://huagongshe.com/reaction/1195752

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantSuronacrineHCID 60601—
ReactantSodium BicarbonateHCID 516892—
CatalystTrifluoroacetic acidHCID 6422—
ProductHCID 54258687HCID 5425868771%

Reaction Steps

To a suspension of 9-benzylamino-1,2,3,4-tetrahydroacridin-1-ol (7.20 g) in 2-bromoethanol (45 ml) was added 40 drops of trifluoroacetic acid. The reaction mixture was stirred at ambient temperature for 20 mins, added to iced sodium bicarbonate solution, and the suspension was extracted with ethyl acetate. The combined organic extracts were washed with water, saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, and evaporated. The residue was purified by flash chromatography (ethyl acetate→1% triethylamine/ethyl acetate) to give 6.85 g (71%) of product. Recrystallization from cyclohexane gave the analytical sample, mp 89°-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112829
Source datasetuspto-grants-1992_05
ORD IDord-16165dbff76a48bc94aff049f7e2aac6
Source noteuspto-grants-1992_05