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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359372Generated: October 31, 2026

Triethylamine → HCID 71227163, compound

https://huagongshe.com/reaction/2359372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantSodiumHCID 5360545—
ReactantHCID 58043115HCID 58043115—
Reactant5-Oxa-2-azaspiro[3.4]octane hydrochlorideHCID 86280355—
SolventDichloromethaneHCID 6344—
ProductHCID 71227163HCID 7122716398.5%

Reaction Steps

To a solution of 4-(1-(5-phenyl-1,3,4-oxadiazole-2-carbonyl)azetidin-3-yloxy)benzaldehyde (70 mg, 0.20 mmol) in dichloromethane (2 mL) was added 5-oxa-2-azaspiro[3.4]octane hydrochloride (80 mg, 0.53 mmol) and triethylamine (0.100 mL, 0.72 mmol). After stirring at ambient temperature for 30 minutes, sodium triacetoxyhydroborate (70 mg, 0.33 mmol) was added. Stirring was continued at ambient temperature overnight, after which NaHCO3 (aq, sat, 5 ml) was added. The phases were separated with the aid of a phase separator. The aqueous phase was extracted twice with dichloromethane and dried with the aid of a phase separator. The combined organic phases were concentrated in vacuo to afford 88 mg of a colourless residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685958B2
Source datasetuspto-grants-2014_04
ORD IDord-29159a8b01e64ee6a1cabda757346737
Source noteuspto-grants-2014_04