HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56254Generated: October 30, 2026
3-Fluoro-4-morpholinoaniline → HCID 72949479, compound
https://huagongshe.com/reaction/56254
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluoro-4-morpholinoaniline | HCID 1485330 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | (Z)-methyl 3-(4-(3-fluorophenoxy)butanamido)but-2-enoate | HCID 90023600 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 72949479 | HCID 72949479 | 49.5% |
Reaction Steps
To a solution of 3-fluoro-4-morpholinoaniline (0.36 g, 1.83 mmol) in DCM (20 mL) was added trimethylaluminium (2.7 mL, 5.40 mmol, 2 M in toluene) and the mixture was stirred at rt for 0.5 h. A solution of (Z)-methyl-3-(4-(3-fluorophenoxy)butanamido)but-2-enoate (0.80 g, 2.71 mmol) in DCM (4 mL) was added slowly and the resulting mixture was stirred at rt for 24 h. The mixture was quenched with saturated NH4Cl aqueous solution and extracted with CH2Cl2 (50 mL×2). The combined organic phases were washed with brine (100 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (EtOAc) to give the title compound as a pale yellow solid (0.40 g, 49%). 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-f50a5f50326c4d1197feded0d938720b |
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| Source note | uspto-grants-2016_09 |
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