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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577273Generated: October 28, 2026

Ethyl Acetate → 2-(2-Bromoethoxy)ethyl 2-fluoro-3-morpholinobenzoate

https://huagongshe.com/reaction/577273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBis(2-bromoethyl) etherHCID 21521—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Amino-2-fluorobenzoic acidHCID 23094343—
SolventDimethylformamideHCID 6228—
Product2-(2-Bromoethoxy)ethyl 2-fluoro-3-morpholinobenzoateHCID 6676517138%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-amino-2-fluorobenzoic acid (500 mg, 3.1 mmol) in DMF (10 mL) was added DIEA (4.5 mL) and 2-bromoethylether (5 eq) and the reaction heated to 80° C. for 18 h. The reaction was allowed to cool to rt, diluted with EtOAc and washed with saturated NH4Cl (aq). The organic phase was dried (Na2SO4), filtered and concentrated in vacuo. The resultant residue was purified by column chromatography (petroleum ether: EtOAc) to give 2-(2-bromoethoxy)ethyl 2-fluoro-3-morpholinobenzoate (450 mg, 38%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040545B2
Source datasetuspto-grants-2015_05
ORD IDord-fed85b1e9e1c4d179e06d2de493b667b
Source noteuspto-grants-2015_05