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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457986Generated: October 29, 2026

Morpholine → 4-Fluoro-2-methoxy-5-morpholin-4-yl-benzoic acid methyl ester

https://huagongshe.com/reaction/457986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 5-bromo-4-fluoro-2-methoxybenzoateHCID 22093493—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product4-Fluoro-2-methoxy-5-morpholin-4-yl-benzoic acid methyl esterHCID 2209349047%

Reaction Conditions

Temperature100 °C

Reaction Steps

In a flame-dried flask, under a nitrogen atmosphere, oven-dried cesium carbonate (4.33 g, 13.3 mmol) was combined with palladium acetate (85.3 mg, 0.380 mmol) and R-(+)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.355 g, 0.570 mmol). While under a constant nitrogen flow, the mixture was dissolved in toluene (0.76 mL) and treated with 5-bromo-4-fluoro-2-methoxy-benzoic acid methyl ester (2.50 g, 9.50 mmol) and morpholine (0.995 mL, 11.4 mmol). After being heated to 100° C. for 24 h, the reaction was cooled to room temperature, diluted with ether, filtered and concentrated. Purification by MPLC (ethyl acetate in heptane) provided 4-fluoro-2-methoxy-5-morpholin-4-yl-benzoic acid methyl ester (1.20 g, 47%): 1H NMR (DMSO-d6 300 MHz) δ 7.33 (d, J=9.9 Hz, 1 H), 7.08 (d, J=14.4 Hz, 1 H), 3.76 (s, 3 H), 3.75 (s, 3 H), 3.70 (t, J=4.7 Hz, 4 H), 2.90 (t, J=4.5 Hz, 4 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189749B2
Source datasetuspto-grants-2007_03
ORD IDord-d718b8a717094237a7bee41e55cc0179
Source noteuspto-grants-2007_03