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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxa-8-aza-spiro[4.5]decane-8-carbonitrileHCID 86678210—
ReactantHCID 178513281HCID 178513281—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product8-(3-Phenyl-1,2,4-oxadiazol-5-yl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 20952653—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822471B2
Source datasetuspto-grants-2014_09
ORD IDord-366afc85b417466a922d9d52cd27e657
Source noteuspto-grants-2014_09