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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694244Generated: October 25, 2026

Nitromethane → 5-((E)-2-Nitro-vinyl)-2-phenoxy-pyridine

https://huagongshe.com/reaction/1694244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantAmmonium AcetateHCID 517165—
Reactant6-PhenoxynicotinaldehydeHCID 2776500—
SolventAcetic AcidHCID 176—
Product5-((E)-2-Nitro-vinyl)-2-phenoxy-pyridineHCID 59255295—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6-phenoxy-pyridine-3-carbaldehyde described in Manufacturing Example 232-1-2 (4.75 g, 23.8 mmol), nitromethane (6.45 mL, 119 mmol), ammonium acetate (3.67 g, 47.6 mmol) and acetic acid (20 mL) was stirred for 3 hours at 100° C. This mixture was cooled to room temperature, and partitioned into ethyl acetate and water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and then filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (5.97 g) as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-9957fbc61bc4486fb29d178561e25b26
Source noteuspto-grants-2012_04