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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691119Generated: November 2, 2026

Acetic Acid → HCID 59255233, compound

https://huagongshe.com/reaction/1691119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantNitromethaneHCID 6375—
ReactantAmmonium AcetateHCID 517165—
Reactant4-(Pyridin-3-yloxy)benzaldehydeHCID 4677419—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 59255233HCID 5925523396.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

To an acetic acid (17.0 mL) solution of 4-(pyridine-3-yloxy)-benzaldehyde (1.70 g, 8.53 mmol) described in Manufacturing Example 76-1-1 were added nitromethane (2.60 g, 42.7 mmol) and ammonium acetate (1.32 g, 17.1 mmol) under nitrogen atmosphere, which was stirred for 3 hours at 110° C. Water and ethyl acetate were added to the reaction solution, and the organic layer was then extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (2.00 g) as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-8e7e9d08377846e4bf5abe7f3f1ffd28
Source noteuspto-grants-2012_04