HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56148Generated: October 29, 2026
2-Butenoic acid, 3-(acetylamino)-, methyl ester, (2Z)- → HCID 72949656, compound
https://huagongshe.com/reaction/56148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Butenoic acid, 3-(acetylamino)-, methyl ester, (2Z)- | HCID 5705360 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 117966053 | HCID 117966053 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 72949656 | HCID 72949656 | 63.2% |
Reaction Steps
To a solution of 2-fluoro-N1,N1-di-n-hexyl benzene-1,4-diamine (0.58 g, 1.97 mmol) in CH2Cl2 (20 mL) was added trimethylaluminum (9.9 mL, 19.8 mmol, 2 M in heptane) slowly at rt. The reaction mixture was stirred at rt for 0.5 h, followed by the addition of a solution of methyl 3-acetaminocrotonate (341 mg, 2.17 mmol) in CH2Cl2 (5 mL). The reaction mixture was stirred at rt for 3 days, then quenched with saturated NH4Cl aqueous solution and extracted with CH2Cl2 (100 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=2:1) to give the title compound as pale yellow oil (500 mg, 63%). The compound was characterized by the following spectroscopic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434695B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-398708dcb06c4f5b99d3a43c59be8a17 |
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| Source note | uspto-grants-2016_09 |
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