HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56182Generated: October 30, 2026
2-Butenoic acid, 3-(acetylamino)-, methyl ester, (2Z)- → HCID 72950003, compound
https://huagongshe.com/reaction/56182
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Butenoic acid, 3-(acetylamino)-, methyl ester, (2Z)- | HCID 5705360 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 28972687 | HCID 28972687 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 72950003 | HCID 72950003 | 27% |
Reaction Steps
To a solution of N1-(3-ethoxypropyl)-2-fluorobenzene-1,4-diamine (5.52 g, 26 mmol) in CH2Cl2 (40 mL) was added trimethylaluminium (52 mL, 104 mmol, 2 M in toluene) slowly. The mixture was stirred at rt for 0.5 h, followed by the addition of a solution of methyl 3-acetaminocrotonate (4.87 g, 31 mmol) in CH2Cl2 (10 mL). The reaction mixture was stirred at rt for 72 h, then quenched with saturated NH4Cl aqueous solution and extracted with CH2Cl2 (150 mL×3). The combined organic phases were washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as pale yellow oil (2.22 g, 27%). 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-480fe4e83a7a401296546e89e8bd87d7 |
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| Source note | uspto-grants-2016_09 |
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