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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273415Generated: November 1, 2026

2-(Ethylamino)ethanol → Ethyl 3-[4-({4'-[2-(ethylamino)ethoxy]-2',6'-dimethylbiphenyl-3-yl}methoxy)-2-fluorophenyl]propanoate

https://huagongshe.com/reaction/273415

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Ethylamino)ethanolHCID 8072—
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 3-{2-fluoro-4-[(4'-hydroxy-2',6'-dimethylbiphenyl-3-yl)methoxy]phenyl}propanoateHCID 58903128—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-[4-({4'-[2-(ethylamino)ethoxy]-2',6'-dimethylbiphenyl-3-yl}methoxy)-2-fluorophenyl]propanoateHCID 5890311889.3%

Reaction Steps

To a solution of ethyl 3-{2-fluoro-4-[(4′-hydroxy-2′,6′-dimethylbiphenyl-3-yl)methoxy]phenyl}propanoate (0.50 g, 1.18 mmol), 2-ethylaminoethanol (0.10 mL, 1.30 mmol) and tributylphosphine (0.44 mL, 1.78 mmol) in tetrahydrofuran (10 mL) was added 1,1′-(azodicarbonyl)dipiperidine (0.45 g, 1.78 mmol) at room temperature with stirring. The reaction mixture was stirred at room temperature for 16 hrs. An equivalent amount of the aforementioned reagents (2-ethylaminoethanol, tributylphosphine and 1,1′-(azodicarbonyl)dipiperidine) were added and the mixture was further stirred at the same temperature for 16 hrs. Diethyl ether was added to the reaction mixture and insoluble material was filtered off. The filtrate was concentrated under reduced pressure and the residue was purified by preparative HPLC (gradient cycle A) to give a colorless oil. The obtained oil was dissolved in ethyl acetate, neutralized with saturated aqueous sodium hydrogen carbonate, washed with water and saturated brine, dried and concentrated under reduced pressure to give the title compound (0.52 g, yield 58%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456218B2
Source datasetuspto-grants-2008_11
ORD IDord-aae70579e81342c28b45cbab763a082c
Source noteuspto-grants-2008_11