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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431745Generated: November 1, 2026

Morpholine → 3-Chloro-5-morpholinoaniline

https://huagongshe.com/reaction/1431745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant3-Bromo-5-chloroanilineHCID 3084709—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-5-morpholinoanilineHCID 59631400—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a stirred solution of 3-bromo-5-chloroaniline (1.00 g, 4.84 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (0.185 g, 0.39 mmol), Pd2dba3 (0.177 g, 0.194 mmol) and morpholine (0.464 g, 5.33 mmol) in tetrahydrofuran (9.7 mL) was added LHMDS in THF (19.37 mL, 19.37 mmol). The resulting mixture was heated to 65° C. and stirring continued for 2.3 h. The reaction was cooled to rt and then poured into water (100 mL) and extracted with EtOAc (2×150 mL) and DCM (2×150 mL). The combined organic layers were dried over magnesium sulfate and the crude product was purified on silica gel (0 to 100% DCM in EtOAc) to give 3-chloro-5-morpholinoaniline. Mass Spectrum (ESI) m/e=213.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-d898171310af477fa35c16ed968f3eb7
Source noteuspto-grants-2015_01