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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791503Generated: October 30, 2026

Tetrahydrofuran → HCID 9969252, compound

https://huagongshe.com/reaction/1791503

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 numberUS07074817B2
Source datasetuspto-grants-2006_07
ORD IDord-611af92e7dae4267bc90a76f838d59bc
Source noteuspto-grants-2006_07