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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095831Generated: November 2, 2026

1,4-Dioxane → 8-[4-(Benzyloxy)phenyl]-1,4-dioxa-8-azaspiro[4,5]decane

https://huagongshe.com/reaction/1095831

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
Reactant1-(Benzyloxy)-4-iodobenzeneHCID 519671—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Dicyclohexylphosphino)biphenylHCID 2734216—
SolventEthyl AcetateHCID 8857—
Product8-[4-(Benzyloxy)phenyl]-1,4-dioxa-8-azaspiro[4,5]decaneHCID 6678391873.6%

Reaction Steps

1,4-Dioxa-8-azaspiro[4,5]decane (653 g, 4.56 mol), 1-(benzyloxy)-4-iodobenzene (1 kg, 3.8 mol), sodium tert-butoxide (511 g, 5.32 mol), Pd(OAc)2 (17 g, 76 mmol) and biphenyl-2-yl(dicyclohexyl) phosphine (54 g, 152 mmol) were mixed, and 1,4-dioxane, this was stirred overnight at 80° C. in a nitrogen atmosphere. The reaction solution was cooled with ice, diluted with ethyl acetate, washed with water and saturated saline in that order, and the organic layer was dried with sodium sulfate. The solvent was evaporated off under reduced pressure, and the resulting residue was purified through silica gel column chromatography (eluate: chloroform/ethyl acetate=10/1), and the resulting crude product was suspended in a mixed solvent of chloroform/hexane and filtered under suction to obtain the entitled compound (910 g, 73%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138206B2
Source datasetuspto-grants-2012_03
ORD IDord-3f38e67ac883422d94ff3de7db0e18b0
Source noteuspto-grants-2012_03