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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691396Generated: October 25, 2026

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

https://huagongshe.com/reaction/1691396

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 numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-c60cd6e24bf54cf89ba3bf4482fd4b7c
Source noteuspto-grants-2012_04