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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582663Generated: October 27, 2026

Aniline → 5-Chloro-2-[(N-phenylamino)acetamido]benzoic Acid

https://huagongshe.com/reaction/582663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Chloro-2-(bromoacetamido)benzoic AcidHCID 10780022—
SolventDimethylformamideHCID 6228—
Product5-Chloro-2-[(N-phenylamino)acetamido]benzoic AcidHCID 10828381—

Reaction Steps

A solution of 5-chloro-2-(bromoacetamido)benzoic acid from Example 41 (10 g, 0.03 mol), aniline (8 g, 7.8 mL, 250 mol %) and DMF (60 mL) was heated at 100-110° C. for 4 h. The reaction mixture was poured into ice-water (200 mL) and the resulting solid product was solubilized by adding 5% KOH (40 mL). The mixture was extracted with CH2Cl2 (3×100 mL) and the aqueous layer was acidified with 5% HBr to pH=3 and extracted with EtOAc (3×200 mL). The EtOAc washings were dried (Na2SO4), filtered and concentrated to afford, after drying under vacuum, 7.8 g (75%) of the title compound as a white solid, mp 210-212° C.; 1H NMR (DMSO-d6) δ 13.99 (s, 1H, NH), 11.96 (s, 1H, COOH), 8.75 (d, 1H, J=8), 7.87 (d, 1H, J=2.8), 7.68 (d, 1H, J=2.4), 7.65 (d, 1H, J=2.8), 7.10 (t, 2H, J=7.6), 6.61 (m, 4H), 3.84 (s, 2H); 13C NMR (DMSO-d6) δ 171.08, 167.81, 148.05, 139.36, 133.81, 130.25, 128.97, 126.20, 121.25, 117.77, 117.14, 112.45, 48.90; MS (EI, m/z) 304 (M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925647
Source datasetuspto-grants-1999_07
ORD IDord-5b1ad19de3f143a1805d2ee97a42d02d
Source noteuspto-grants-1999_07