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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847115Generated: October 31, 2026

Thionyl Chloride → HCID 50898388, compound

https://huagongshe.com/reaction/1847115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86667487HCID 86667487—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 50898388HCID 5089838828%

Reaction Steps

Compound 3 (41.5 mg, 0.0999 mmol) obtained in Example 3 was dissolved in 1,4-dioxane (3.0 mL), and thionyl chloride (21.9 μL, 0.300 mmol) was added thereto at room temperature, followed by stirring for 1 hour. A saturated aqueous sodium bicarbonate solution was added to the reaction mixture, followed by extraction with ethyl acetate twice. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to yield a residue. The residue was purified by preparative thin layer chromatography to obtain the title compound (11.6 mg, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952003B2
Source datasetuspto-grants-2015_02
ORD IDord-8b424a794fd34442ace64fb08d4d8c3d
Source noteuspto-grants-2015_02