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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219784Generated: October 26, 2026

Morpholine → Methyl 3-methyl-4-morpholin-4-ylbenzoate

https://huagongshe.com/reaction/219784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 4-bromo-3-methylbenzoateHCID 3294148—
Catalystpalladium(II) acetateHCID 167845—
CatalystBinap, (A+-)-HCID 634876—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 3-methyl-4-morpholin-4-ylbenzoateHCID 6752885884%

Reaction Steps

To a stirred solution of methyl 4-bromo-3-methylbenzoate (5 g, 21.8 mmol) in dry 1,4-dioxane (100 mL), were added dry Cs2CO3 (10.65 g, 32.7 mmol) and morpholine (2.3 g, 26 mmol). The mixture was degassed for 10 min. BINAP (0.67 g, 1.1 mmol) and palladium(II)acetate (0.24 g, 1.1 mmol) were added under N2 and the resulting mixture was refluxed for 15 h. The reaction mixture was filtered through a pad of celite and the filtrate was evaporated. The crude product was purified by flash chromatography, affording the title compound as a yellow solid (4.3 g, 84%). 1H NMR (CDCl3, 400 MHz) δ 7.86-7.90 (m, 2H), 7.13-7.16 (d, 1H), 3.98-4.0 (m, 4H), 3.91 (3H, s), 3.10-312 (m, 4H), 2.45 (3H, s). LC/MS (Method A): 236.0 (M+H)+. HPLC (Method B) Rt 2.24 min (Purity: 95.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-1e594bfb65c4447a9bc2133b32bd3085
Source noteuspto-grants-2012_06