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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988199Generated: November 2, 2026

Tetrahydrofuran → 3-(5-Amino-1,3,4-oxadiazol-2-yl)pentan-3-ol

https://huagongshe.com/reaction/1988199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 5-amino-1,3,4-oxadiazole-2-carboxylateHCID 2756523—
ReactantHCID 178418443HCID 178418443—
Product3-(5-Amino-1,3,4-oxadiazol-2-yl)pentan-3-olHCID 57437839—

Reaction Steps

To a solution of ethyl magnesium bromide (200 mmol) in 300 mL of THF at 0° C. was added a suspension of ethyl 5-amino-1,3,4-oxadiazol-2-carboxylate (8.00 g, 50.9 mmol; Chemical Abstract, 1966, 64, 3558a) in THF. The reaction mixture was brought to rt and 30 min later quenched with NH4Cl. After extraction with EtOAc and drying over MgSO4, the solvent was removed. The crude product thus obtained was triturated, filtered and dried to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553973B2
Source datasetuspto-grants-2009_06
ORD IDord-a93b1789eefe4102a66dfa592b1475df
Source noteuspto-grants-2009_06