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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539158Generated: October 27, 2026

Morpholine → N-(2-methoxy-4-morpholino-6-nitrophenyl)acetamide

https://huagongshe.com/reaction/539158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantBinap, (A+-)-HCID 634876—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-(4-bromo-2-methoxy-6-nitrophenyl)acetamideHCID 53491145—
Solvent1,4-DioxaneHCID 31275—
ProductN-(2-methoxy-4-morpholino-6-nitrophenyl)acetamideHCID 6697701935%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of N-(4-bromo-2-methoxy-6-nitrophenyl)acetamide (2.89 g), morpholine (2.61 g), BINAP (1.21 g) and t-BuOK (1.53 g) in dioxane (50 mL) was degassed with N2 and the mixture was stirred at 110° C. in a sealed tube overnight. It was cooled to room temperature and filtered. The filtrate was concentrated in-vacuo. The residue was purified by silica gel chromatography eluted with MeOH/DCM=1/50 to afford the desired product (1.03 g, 35%) 1H NMR (300 MHz, CDCl3) δ ppm 2.15 (s, 1H), 3.18 (t, 4H, J=4.8 Hz), 3.85 (t, 4H, J=4.8 Hz), 3.88 (s, 3H), 6.63 (d, 1H, J=2.7 Hz), 6.96 (d, 1H, J=2.7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865912B2
Source datasetuspto-grants-2014_10
ORD IDord-2e37d1dc13814f71a99bb71035d4bb09
Source noteuspto-grants-2014_10