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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509850Generated: October 30, 2026

2,3-Dihydro[1,4]dioxino[2,3-c]pyridine-7-carbaldehyde → 2,3-Dihydro[1,4]dioxino[2,3-c]pyridine-7-carboxylic acid

https://huagongshe.com/reaction/1509850

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydro[1,4]dioxino[2,3-c]pyridine-7-carbaldehydeHCID 21873668—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Solvent2-Methyl-2-buteneHCID 10553—
Product2,3-Dihydro[1,4]dioxino[2,3-c]pyridine-7-carboxylic acidHCID 2187362451.2%

Reaction Steps

To a solution of 2,3-dihydro-[1,4]dioxino[2,3-c]pyridine-7-carbaldehyde (722 mg, 4.37 mmol) in 2-methyl-2-propanol (95 mL) and 2-methyl-2-butene (22 mL) was added dropwise a solution of sodium chlorite (80%, 4.55 g, 40.22 mmol) and sodium dihydrogenphosphate (3.65 g, 26.45 mmol) in water (35 mL). The resulting solution was stirred at rt for 19 h. The volatiles were removed under reduced pressure. The residue was diluted with water (20 mL) and pH was adjusted to 3 by addition of 1N HCl. The aq. layer was extracted with DCM-MeOH 9-1 (25×30 mL). The combined extracts were dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was triturated in ether and filtered to give the title acid as a white solid (0.405 g, 51% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211890B2
Source datasetuspto-grants-2012_07
ORD IDord-2829e531b0f64600bf5277c9951c20fb
Source noteuspto-grants-2012_07