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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224701Generated: October 30, 2026

p-Fluoronitrobenzene → HCID 59717865, compound

https://huagongshe.com/reaction/2224701

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantCesium carbonateHCID 10796—
Reactanttert-butyl N-(2-(4-hydroxyphenyl)ethyl)carbamateHCID 11831452—
SolventDimethylformamideHCID 6228—
ProductHCID 59717865HCID 5971786586.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

Combine [2-(4-Hydroxy-phenyl)-ethyl]-carbamic acid tert-butyl ester (1.0 g, 4.2 mmol), 4-fluoronitrobenzene (0.6 g, 4.2 mmol), cesium carbonate (2.7 g, 8.4 mmol), and N,N-dimethylformamide (35 mL), stir and heat at 100° C. for 18 hours. Cool to room temperature and evaporate on a rotary evaporator to yield the crude product (9.5 g). The crude product is purified by flash column chromatography on silica gel eluting with (10% conc. ammonium hydroxide in ethanol) and chloroform to yield {2-[4-(4-nitro-phenoxy)-phenyl]-ethyl}-carbamic acid tert-butyl ester (1.3 g): 1H NMR (CDCl3, 300.00 MHz): 8.23 (d, 2H, J=9.2 Hz), 7.32-7.25 (m, 2H), 7.10-7.00 (m, 4H), 4.63 (s, 1H), 3.43 (m, 2H), 2.86 (t, 2H, J=7.0 Hz), 1.48 (s, 9H). Step 3 {2-[4-(4-Amino-phenoxy)-phenyl]-ethyl}-carbamic acid tert-butyl ester

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378448B2
Source datasetuspto-grants-2008_05
ORD IDord-a9a3b266312d4c109065de16abbca3a3
Source noteuspto-grants-2008_05