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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant18-Crown-6HCID 28557—
ReactantPotassium FluorideHCID 522689—
ReactantBenzyl 2-(3-iodyl-4-nitrobenzamido)acetateHCID 86713123—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 2-(3-fluoro-4-nitrobenzamido)acetateHCID 8671312261%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906344B2
Source datasetuspto-grants-2014_12
ORD IDord-bd08398fce0a47cfa060711fdbaaa270
Source noteuspto-grants-2014_12