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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221279Generated: November 1, 2026

Tetrahydrofuran → HCID 9969252, compound

https://huagongshe.com/reaction/2221279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22032982HCID 22032982—
ProductHCID 9969252HCID 9969252—

Reaction Steps

The product from Step 3 of Example 45 was dissolved in 0.5 ml anhydrous THF and 50 μL (COCl)2 was added. The solution was mixed at room temperature overnight with orbital shaking. An aliquot removed for LC analysis indicated that the reaction was complete. The solution was added to 1 mL aqueous NaHCO3 and the vial was capped and shaken. 0.1 mL 2N HCl was added and the vial was again capped and shaken. The reaction was concentrated to dryness under vacuum. The residue was purified by RP-HPLC (see Note 1 below) to give 6.4 mg of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368471B2
Source datasetuspto-grants-2008_05
ORD IDord-31122e0e5d584939a4578c8b3564672d
Source noteuspto-grants-2008_05