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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582667Generated: October 30, 2026

Anthranilic Acid → N-(2-Carboxyphenyl)phenoxyacetamide

https://huagongshe.com/reaction/582667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthranilic AcidHCID 227—
ReactantHydrochloric AcidHCID 313—
ReactantPhenoxyacetyl chlorideHCID 69703—
SolventSodium HydroxideHCID 14798—
ProductN-(2-Carboxyphenyl)phenoxyacetamideHCID 9932581.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of anthranilic acid (5 g, 0.036 mol) in NaOH (3 g, 30 mL) was added phenoxyacetyl chloride (6.2 g, 5.2 mL) dropwise at 0° C. The reaction mixture was stirred at 0° C. for 30 min, acidified with dilute hydrochloric acid and filtered. The filtered solid was dissolved in EtOAc and filtered. The filtrate was dried, filtered, concentrated and dried for 4 h under vacuum, affording 8 g (81%) of the title compound, mp 201-203° C. A small amount (100 mg) of the title compound was recrystallized from EtOH, affording 75 mg of the title compound, mp 202-203° C.; 1H NMR (DMSO-d6) δ 13.70 (s, 1H, COOH), 12.20 (s, 1H, NH), 8.71 (d, 1H, J=8.4), 8.02 (dd, 1H, J=7.6), 7.65-7.60 (m, 1H), 7.35-6.89 (m, 6H), 4.73 (s, 2H); 13C NMR (DMSO-d6) δ 169.44, 167.23, 157.11, 140.22, 134.34, 131.32, 129.65, 129.45, 123.06, 121.65, 120.96, 119.45, 116.14, 114.81, 114.38, 67.22; MS (EI, m/z) 271 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925647
Source datasetuspto-grants-1999_07
ORD IDord-178e53264de449589452a507f1c59730
Source noteuspto-grants-1999_07