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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 1,4-Dioxa-8-azaspiro(4.5)decane | HCID 67435 | — |
| Reactant | 1-(Benzyloxy)-4-iodobenzene | HCID 519671 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 8-[4-(Benzyloxy)phenyl]-1,4-dioxa-8-azaspiro[4,5]decane | HCID 66783918 | 73.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138206B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-3f38e67ac883422d94ff3de7db0e18b0 |
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| Source note | uspto-grants-2012_03 |
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