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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987219Generated: November 1, 2026

Acetamide, N-(4-fluoro-3-nitrophenyl)- → HCID 57441096, compound

https://huagongshe.com/reaction/1987219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamide, N-(4-fluoro-3-nitrophenyl)-HCID 67694—
ReactantHCID 57441095HCID 57441095—
SolventEthanolHCID 702—
ProductHCID 57441096HCID 57441096—

Reaction Steps

N-(4-Fluoro-3-nitrophenyl)acetamide (460 mg, 2.32 mmol) and [(4-fluorocyclohex-3-en-1-yl)methyl]amine hydrochloride (350 mg, 2.11 mmol) were stirred in 20 mL of EtOH containing TEA (0.735 mL, 5.28 mmol) at 75° C. for 48 h. The solvent was concentrated. The residue was dissolved in EtOAc and washed with aqueous 5% KHSO4, saturated aqueous NaHCO3 solution, brine and dried over anhydrous MgSO4. The crude product was purified by silica gel flash chromatography using 2:1/hexanes:acetone as eluent. Yield: 553 mg (85%). 1H NMR (400 MHz, CHLOROFORM-D) δ 1.51-1.61 (m, 1 H), 1.84-1.93 (m, 1 H), 1.96-2.03 (m, 2 H), 2.16-2.18 (m, 3 H), 2.22-2.32 (m, 3 H), 3.26 (m, 2 H), 5.19 (m, 1 H), 6.84 (d, J=9.37 Hz, 1 H), 7.21 (s, 1 H), 7.79 (dd, J=9.18, 2.54 Hz, 1 H), 8.09 (d, J=2.54 Hz, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550495B2
Source datasetuspto-grants-2009_06
ORD IDord-e4b37739948d4fea800bee6c82111a0c
Source noteuspto-grants-2009_06