Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269641Generated: October 29, 2026

Ethyl bromoacetate → Ethyl 1-naphthylaminoacetate

https://huagongshe.com/reaction/2269641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant1-NaphthylamineHCID 8640—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1-naphthylaminoacetateHCID 18347840—

Reaction Steps

In 5 ml of THF, 500 mg of 1-naphthylamine was added, then 168 mg of sodium hydride (60% in oil) was added and the resultant mixture was stirred for 30 min under ice cooling. To the reaction mixture, 0.46 ml of ethyl bromoacetate was added and the mixture was refluxed for 5 hr. The reaction mixture was evaporated under reduced pressure and the resultant residue was re-dissolved in ethyl acetate. The obtained solution was washed with 5% sodium hydrogencarbonate aqueous solution and saturated sodium chloride aqueous solution, successively, and dried over anhydrous sodium sulfate. The dried solution was evaporated under reduced pressure and subjected to a silica gel column chromatography (n-hexane:ethyl acetate=10:1) to give 720 mg of ethyl 1-naphthylaminoacetate. In 10 ml of ethanol, 460 mg of the ester was dissolved, 3.78 ml of 1N—NaOH aqueous solution was added and the resultant mixture was stirred for 1 hr. The reaction mixture was evaporated under reduced pressure, neutralized by the addition of 1N—HCl and extracted with ethyl acetate. The extract was washed with saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The dried solution was evaporated under reduced pressure and crystallized by the treatment with ether to give 188 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329502B1
Source datasetuspto-grants-2001_12
ORD IDord-9ecf8957a4e9432b8e94849f1d1ee2e9
Source noteuspto-grants-2001_12