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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457957Generated: October 30, 2026

HCID 18468176, compound → HCID 12968791, compound

https://huagongshe.com/reaction/457957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18468176HCID 18468176—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 12968791HCID 1296879172.1%

Reaction Steps

[2-(4-Bromo-2-fluoro-benzylcarbamoyl)-4-nitro-phenoxy]-acetic acid (1.10 g, 2.76 mmol) was dissolved in ethyl alcohol (40 mL, 0.1 M), treated with 10% Pd on carbon (Degussa, 0.10 g) and placed under a balloon of hydrogen for 12 h. The reaction was filtered through Celite and concentrated to give a crude solid which was recrystallized from heptane and ethyl acetate to give [4-amino-2-(4-bromo-2-fluoro-benzylcarbamoyl)-phenoxy]-acetic acid (0.79 g, 66%): mp 204° C. (dec.); Rf 0.10 (10% methanol in dichloromethane); 1H NMR (DMSO-d6, 300 MHz) δ 9.16 (br t, J=6.3 Hz, 1 H), 7.85 (d, J=2.7 Hz, 1 H), 7.46–7.11 (m, 5 H), 4.91 (s, 2 H), 4.57 (br d, J=3.6 Hz, 2 H). ESI-LC/MS m/z calcd for C16H14BrFN2O4: 396.0 found 395.0 (M−1)−. Anal. calcd for C16H14BrFN2O4: C, 48.38; H, 3.55; N, 7.05. Found C, 48.05; H, 4.02; N, 6.94.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189749B2
Source datasetuspto-grants-2007_03
ORD IDord-767c5e6be7bc46cbab58b7a20901a4df
Source noteuspto-grants-2007_03