Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | HCID 58562838 | HCID 58562838 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58562553 | HCID 58562553 | — |
Reaction Steps
A solution of 8-(1-(allyloxy)but-3-en-1-yl)-1,4-dioxaspiro[4.5]decane (454 mg, 1.80 mmol), prepared in the previous step, and the Grubbs Generation II catalyst (76 mg, 0.09 mmol) in DCM was degassed and heated to 40° C. under argon for 4 hours. After extraction with saturated NaHCO3 solution, the organic layer was concentrated in vacuo and the residue purified by flash chromatography (silica gel, ether) to afford the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062048B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-491bb316676241759930c737edc72a63 |
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| Source note | uspto-grants-2015_06 |
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