HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399450Generated: November 2, 2026
Acetonitrile → Benzyl 2-(3-fluoro-4-nitrobenzamido)acetate
https://huagongshe.com/reaction/1399450
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Benzyl 2-(3-iodyl-4-nitrobenzamido)acetate | HCID 86713123 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl 2-(3-fluoro-4-nitrobenzamido)acetate | HCID 86713122 | 61% |
Reaction Steps
A mixture of spray-dried KF (614 mg, 10.59 mmol), intermediate 7 (1 g, 2.12 mmol), 18-crown-6 (40 mg) and dry acetonitrile (20 mL) was refluxed for 40 min. After completion of reaction (TLC), the mixture was diluted with EtOAc (75 mL). The solution was successively washed with water (50 mL) and brine (50 mL) and dried over anhyd Na2SO4. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using chloroform:hexane (75:25) as eluents to give the product as a colorless solid (430 mg, 61%), mp 118-120° C. 1H NMR (400 MHz, CDCl3): δ 8.13 (1H, t, J=7.8 Hz), 7.75 (1H, d, J=10.8 Hz), 7.68 (1H, d, J=8.0 Hz), 7.38 (5H, br s), 6.68 (1H, br s), 5.25 (2H, s), 4.29 (2H, d, J=4.8 Hz); LC-MS negative ion mode): m/z 331 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906344B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-bd08398fce0a47cfa060711fdbaaa270 |
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| Source note | uspto-grants-2014_12 |
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