HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68756Generated: October 25, 2026
1,4-Dioxa-8-aza-spiro[4.5]decane-8-carbonitrile → 8-(3-Phenyl-1,2,4-oxadiazol-5-yl)-1,4-dioxa-8-azaspiro[4.5]decane
https://huagongshe.com/reaction/68756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxa-8-aza-spiro[4.5]decane-8-carbonitrile | HCID 86678210 | — |
| Reactant | HCID 178513281 | HCID 178513281 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 8-(3-Phenyl-1,2,4-oxadiazol-5-yl)-1,4-dioxa-8-azaspiro[4.5]decane | HCID 20952653 | — |
Reaction Steps
A 0.5 M solution of zinc chloride in tetrahydrofuran (18.00 mL) is added dropwise at room temperature to a mixture of N-hydroxy-benzamidine (817 mg) and 1,4-dioxa-8-aza-spiro[4.5]decane-8-carbonitrile (1.00 g) in ethyl acetate (20 mL). The reaction mixture is stirred at 50° C. for 3 h and cooled to room temperature. The precipitate is filtered off and heated to 100° C. for 1 h in a mixture of ethanol (10 mL) and glacial acetic acid (5 mL). The solvents are evaporated and the crude product is purified by HPLC. TLC: rf=0.88 (silica gel, CH2Cl2/MeOH 9:1); Mass spectrum (ESI+): m/z=288 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822471B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-366afc85b417466a922d9d52cd27e657 |
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| Source note | uspto-grants-2014_09 |
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