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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502885Generated: November 2, 2026

Ethyl Acetate → 2-(2-Nitro-5-phenoxy-benzyl)-hex-5-enenitrile

https://huagongshe.com/reaction/502885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHeptaneHCID 8900—
Reactant2-Cyano-2-(2-nitro-5-phenoxy-benzyl)-hex-5-enoic acidHCID 57475718—
SolventDimethylacetamideHCID 31374—
Product2-(2-Nitro-5-phenoxy-benzyl)-hex-5-enenitrileHCID 57475719—

Reaction Conditions

Temperature150 °C

Reaction Steps

To a round bottom flask equipped with a stir bar, condenser, and a nitrogen inlet 2-cyano-2-(2-nitro-5-phenoxy-benzyl)-hex-5-enoic acid (4.0 g, 10.92 mmol) was added and dissolved in dimethylacetamide (10 mL). The solution was heated to 150° C. for 3 hours. The reaction mixture was allowed to room temperature, then the solvent was removed under reduced pressure. The resulting crude product was dissolved in ethyl acetate and washed 3 times with 1N HCl followed by one wash with saturated brine solution. The organic layer was separated and dried with anhydrous sodium sulfate and the solvent was removed to yield crude material. The crude material was subjected to flash chromatography (mobile phase 9:1 heptane:ethyl acetate) to yield a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776882B2
Source datasetuspto-grants-2010_08
ORD IDord-16ec7119c7d44877915d0e90f8caae53
Source noteuspto-grants-2010_08