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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095384Generated: October 26, 2026

Morpholine → N-(2-methoxy-6-nitrophenyl)-2-morpholin-4-ylacetamide

https://huagongshe.com/reaction/1095384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant2-bromo-N-(2-methoxy-6-nitrophenyl)acetamideHCID 57436027—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-methoxy-6-nitrophenyl)-2-morpholin-4-ylacetamideHCID 5743602875.6%

Reaction Steps

To a solution of 2-bromo-N-(2-methoxy-6-nitrophenyl)acetamide (Step 1, 8.8 g, 30 mmol) in THF (240 mL) was added morpholin (11 mL, 122 mmol) at 0° C. and warmed to rt. After 2.5 h, the reaction mixture was quenched by addition of water (200 mL) and extracted with ethyl acetate (200 mL×2). The combined organic layers were washed with water (200 mL), brine (100 mL) dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with hexane/ethyl acetate (2/1) to afford 6.7 g (75%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138177B2
Source datasetuspto-grants-2012_03
ORD IDord-184fbfc0ca2f49c98231e4027798ca7a
Source noteuspto-grants-2012_03