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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911060Generated: October 25, 2026

Lithium Hexamethyldisilazide → 4-(benzyloxy)pyridin-2-amine

https://huagongshe.com/reaction/911060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant4-(Benzyloxy)-2-chloropyridineHCID 53404197—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
Product4-(benzyloxy)pyridin-2-amineHCID 52008470.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

4-(benzyloxy)-2-chloropyridine (18.6 g, 84.7 mmol), XPHOS (4.04 g, 8.47 mmol), and Pd2dba3 (3.88 g, 4.23 mmol) were mixed in THF (250 mL). LHMDS (93.1 ml, 93.1 mmol) was added and the reaction was heated at 50° C. for 1.5 hours. The solution was cooled and diluted with 1N HCl (50 mL) and stirred at ambient temperature for 2 hours. The reaction was concentrated and the residue was extracted with EtOAc. The aqueous layer was basified with saturated K2CO3 and the aqueous layer was extracted with EtOAc. The combined organic layers were dried and concentrated to give the desired product (11.9 g, 70.2% yield) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022222B2
Source datasetuspto-grants-2011_09
ORD IDord-fa84e86061a148fe8272fc9c06874a48
Source noteuspto-grants-2011_09