HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75347Generated: October 28, 2026
2-Fluoroaniline → N-(2-Fluorophenyl) cinnamamide
https://huagongshe.com/reaction/75347
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoroaniline | HCID 9584 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Phenylprop-2-enoyl chloride | HCID 66023 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-Fluorophenyl) cinnamamide | HCID 303250 | 103.2% |
Reaction Steps
To a solution of 2-fluoroaniline (25.0 g, 225 mmol) and potassium carbonate (47 g, 337 mmol) in water (112 mL) and acetone (45 mL) at 0° C. was added cinnamoyl chloride (37.0 g, 225 mmol, 1 eq) in acetone (45 mL) over 2 h. The reaction was stirred for 1 h at 0° C., and quenched into 200 mL of ice-water. The white crystalline solid was filtered and washed with water. The solid was air dried for 2 h, then washed with 400 mL of hexanes. The solid was dried under vacuum overnight to afford N-(2-fluorophenyl)cinnamamide (56 g, 103% yield). 1H NMR (400 MHz, CDCl3) δ ppm 8.49 (br t, J=7.8 Hz, 1H), 7.80 (d, J=15.3 Hz, 1H), 7.57 (m, 3H), 7.41 (m, 3H), 7.17 (m, 3H), 6.61 (d, J=15.6 Hz, 1H). Mass Spectrum (ESI) m/e=242.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835432B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-822acde15eb6429c8fb14d5a281c40fb |
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| Source note | uspto-grants-2014_09 |
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