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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782175Generated: November 1, 2026

Potassium Carbonate → Diethyl 2-(3-ethynylphenylamino)ethylphosphonate

https://huagongshe.com/reaction/1782175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDiethyl (2-bromoethyl)phosphonateHCID 79218—
ReactantBenzenamine, 3-ethynyl-HCID 104682—
SolventAcetonitrileHCID 6342—
ProductDiethyl 2-(3-ethynylphenylamino)ethylphosphonateHCID 575884287.2%

Reaction Steps

3-Ethynyl aniline (2.36 g, 22.1 mmol), diethyl 2-bromoethylphosphonate (5.41 g, 22.1 mmol) and potassium carbonate (3.1 gm, 22.1 mmol) were heated at 90° C. in anhydrous acetonitrile (40 mL) for 26 h. The solvent was removed under reduced pressure and the residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by flash column chromatography on silica gel, eluting with 1:1 ethyl acetate:hexanes followed by 97:3 methylene chloride:methanol to provide diethyl 2-(3-ethynylphenylamino)ethylphosphonate (450 mg) as a yellow oil. 1H NMR (CDCl3) δ 7.15 (t, 1H), 6.83 (d, 1H), 6.70 (br s, 1H), 6.60 (m, 1H), 4.10 (m, 4H), 3.41 (m, 2H), 3.00 (s, 1H), 2.10 (m, 2H), 1.35 ppm (m, 6H). MW=281 confirmed by LC-MS, tr=11.65 min (Method Y) MH+=282.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498353B2
Source datasetuspto-grants-2009_03
ORD IDord-8afee5cf262241de8d877b4321071517
Source noteuspto-grants-2009_03