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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 2-Cyano-2-(2-nitro-5-phenoxy-benzyl)-hex-5-enoic acid | HCID 57475718 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 2-(2-Nitro-5-phenoxy-benzyl)-hex-5-enenitrile | HCID 57475719 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776882B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-16ec7119c7d44877915d0e90f8caae53 |
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| Source note | uspto-grants-2010_08 |
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