Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640574Generated: October 25, 2026

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

https://huagongshe.com/reaction/640574

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 numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-c96db83f024145a6a922371d9db9a9d0
Source noteuspto-grants-2010_04