HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598176Generated: October 25, 2026
Acetic Anhydride → (E)-2-(2,6-dichlorobenzoyl)-3-(1-propylbutylamino)acrylonitrile
https://huagongshe.com/reaction/598176
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 4-Heptanamine | HCID 38665 | — |
| Reactant | 3-(2,6-Dichlorophenyl)-3-oxopropiononitrile | HCID 3018140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (E)-2-(2,6-dichlorobenzoyl)-3-(1-propylbutylamino)acrylonitrile | HCID 67267339 | 10.5% |
Reaction Steps
A mixture of 3-(2,6-dichlorophenyl)-3-oxopropanenitrile (0.200 g, 0.93 mmol), acetic anhydride (0.22 g, 2.20 mmol), and triethyl orthoformate (0.21 g, 1.40 mmol) was stirred at 150° C. for 1 hr. The solution was then concentrated and the residue redissolved in ethanol (5 mL). 4-heptylamine (0.16 g, 1.4 mmol) in 1 mL of tetrahydrofuran was added to the reaction mixture at 0° C. The reaction stirred for 30 minutes and was then concentrated. Flash chromatography (20% Ethyl acetate/hexanes) gave the desired compound (0.033 g, 10%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897607B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-c02c2c1bc69342f3afc648452bc0ea63 |
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| Source note | uspto-grants-2011_03 |
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