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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582664Generated: October 30, 2026

Aniline → HCID 18929250, compound

https://huagongshe.com/reaction/582664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 18929201HCID 18929201—
SolventDimethylformamideHCID 6228—
ProductHCID 18929250HCID 1892925082%

Reaction Steps

A solution of 6-chloro-2-(bromoacetamido)benzoic acid from Example 42 (7 g, 0.024 mol), aniline (5.6 g, 6 mL, 250 mol %) and DMF (40 mL) was heated at 100° C. for 5 h. The reaction mixture was cooled to rt, poured onto ice and the resulting crystalline product was solubilized by adding 5% KOH (70 mL, pH=9). The resulting milky homogenous solution was extracted with CH2Cl2 (3×100 mL), and the aqueous layer was acidified to pH=3 with 5% HBr and extracted with EtOAc (4×100 mL). Combined EtOAc washings were dried and concentrated. Recrystallization of the resulting solid from EtOAc/Hex, afforded 6 g (82%) of the title compound as white crystals, 176-178.2° C.; 1H NMR (DMSO-d6) δ 9.93 (s, 1H, COOH), 7.97 (d, 1H, J=8), 7.42 (t, 1H, J=8), 7.30 (d, 1H, J=7.6), 7.12 (t, 2H, J=7.2), 6.65 (t, 3H, J=7.2), 3.82 (s, 2H); 13C NMR (DMSO-d6) δ 170.19, 166.30, 148.15, 136.56, 131.12, 130.53, 128.98, 125.51, 121.39, 117.23, 112.71, 48.13; MS (EI, m/z) 304 (M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925647
Source datasetuspto-grants-1999_07
ORD IDord-9db803662b7f4522a84ffc9a62755062
Source noteuspto-grants-1999_07