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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465456Generated: November 3, 2026

Pyridine → HCID 67030046, compound

https://huagongshe.com/reaction/1465456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 67030367HCID 67030367—
SolventDichloromethaneHCID 6344—
ProductHCID 67030046HCID 6703004692%

Reaction Steps

To a mixture of N-(4-bromophenyl)-N-ethylethane-1,2-diamine dihydrochloride (1.044 g, corresponding to 2.33 mmol), pyridine (4 ml) and anhydrous dichloromethane (8 ml) was added dropwise acetic anhydride (0.28 ml, 2.92 mmol) at 0° C. After stirring at room temperature for 70 mins, the reaction mixture was diluted with dichloromethane (50 ml), washed twice with diluted aqueous sodium hydrogen carbonate solution and with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:4→1:0) to give N-{2-[(4-bromophenyl)(ethyl)amino]ethyl}acetamide (460 mg, overall yield of 2 steps 92%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-0279054c1e5f48e0b6595d05c3cb27d5
Source noteuspto-grants-2015_04