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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359382Generated: November 2, 2026

Triethylamine → HCID 71227171, compound

https://huagongshe.com/reaction/2359382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantSodiumHCID 5360545—
ReactantHCID 86690184HCID 86690184—
Reactant1419590-65-0HCID 131731278—
SolventDichloromethaneHCID 6344—
ProductHCID 71227171HCID 7122717162.6%

Reaction Steps

2-Oxa-5-azaspiro[3.4]octane TFA salt (0.1.1 g, ca. 70%, 0.34 mmol) and 4-(1-(5-(4-(difluoromethyl)phenyl)-1,3,4-oxadiazole-2-carbonyl)azetidin-3-yloxy)-3-methoxybenzaldehyde (0.146 g, 0.34 mmol) were mixed in dichloromethane (2 ml). Triethylamine (0.1 ml, 0.72 mmol) was added, followed by sodium triacetoxyhydroborate (0.144 g, 0.68 mmol). The mixture was stirred at ambient temperature overnight (16 h). LC-MS showed some remaining starting material and an additional amount of sodium triacetoxyhydroborate (0.113 g) was added. Stirring continued for 6 h. The reaction mixture was then diluted with dichloromethane (10 ml) and shaken with NaHCO3 (sat. 3 ml). The two phases were separated by the use of a phase separator. Evaporation of the organic phase afforded a residue, which was purified by preparative reverse-phase HPLC at pH 10 to give 0.112 g (62%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685958B2
Source datasetuspto-grants-2014_04
ORD IDord-54a7929a10ea4dfbb9974f9fe7466191
Source noteuspto-grants-2014_04