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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889271Generated: October 29, 2026

Ethyl Acetate → Methyl 2-(2-benzyloxy-6-fluoroanilino)-acetate

https://huagongshe.com/reaction/889271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl bromoacetateHCID 60984—
ReactantHCID 15219197HCID 15219197—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(2-benzyloxy-6-fluoroanilino)-acetateHCID 68430918—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-benzyloxy-6-fluoroaniline (950 mg, 4.37 mmol), methyl bromoacetate (456 μL, 737 mg, 4.82 mmol), and potassium carbonate (1.21 g, 8.76 mmols) in DMF (10 mL) is heated at 60° C. for 18 h. The mixture is poured into ethyl acetate and extracted once with water and five times with brine. The organic layer is dried, filtered, and the solvent removed under reduced pressure to afford a crude oil that is chromatographed on an Isco Companion (80 g silica gel, 0-30% gradient of hexane/ethyl acetate) to afford methyl 2-(2-benzyloxy-6-fluoroanilino)-acetate as an oil. MS (M+1)+=290; NMR (CDCl3): δ 7.39 (m, 5H), 6.67 (m, 3H), 5.10 (s, 2H), 4.57 (br s, 1H), 4.11 (m, 2H), 3.72 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252820B2
Source datasetuspto-grants-2012_08
ORD IDord-84bc523a57de4e5baf62d1c7e360d8fe
Source noteuspto-grants-2012_08