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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432422Generated: November 2, 2026

Sodium Nitrite → HCID 136335130, compound

https://huagongshe.com/reaction/1432422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium NitriteHCID 23668193—
Reactant1-(1,3-benzodioxol-5-yl)-2-(6-methyl-2-pyridinyl)EthanoneHCID 68885000—
SolventAcOH THF waterHCID 21877175—
ProductHCID 136335130HCID 13633513081%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium nitrite (0.405 g, 5.88 mmol) was added to a solution of 1-benzo[1,3]dioxol-5-yl-2-(6-methyl-pyridin-2-yl)-ethanone (1.0 g, 3.92 mmol; see Example 3B above) in a mixture of HOAc/THF/H2O (6:4:1, 22 mL). The mixture was stirred at 0° C. for 1 hour and then at room temperature for 1 hour. Solvent was removed under reduced pressure. Residue was dissolved in water and NaOH (3N) was added until the pH value was more than 8. The aqueous solution was then extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, filtered, and concentrated to give 0.90 g (81%) of 1-Benzo[1,3]dioxol-5-yl-2-(6-methyl-pyridin-2-yl)ethane-1,2-dione 2-oxime as a yellow foam. MS (ESP+) m/z 285.1 (M+1). 1H NMR (300 MHz, CDCl3) δ 7.49 (m, 4H), 7.09 (d, 1H, J=7.5 Hz), 6.81 (d, 1H, J=7.8 Hz), 6.04 (s, 2H), 2.43 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612094B2
Source datasetuspto-grants-2009_11
ORD IDord-bd7bc32f912948f2ae6bd58fe880930a
Source noteuspto-grants-2009_11