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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350357Generated: October 31, 2026

Hydrochloric Acid → HCID 23511825, compound

https://huagongshe.com/reaction/350357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactantbenzyl 4-[N'-(2-fluorophenyl)ureido]-3-methoxyphenylacetateHCID 23512303—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23511825HCID 2351182566%

Reaction Steps

To a stirred solution of benzyl 4-[N′-(2-fluorophenyl)ureido]-3-methoxyphenylacetate (2.04 g, 5 mmol) in THF (40 mL) was added 0.25 N NaOH (40 mL). The resulting mixture was stirred overnight. The mixture was poured into 1 N HCl (10 mL), and the resulting precipitate was collected with suction. The residue was recrystallized from CHCl3-EtOH to give 1.04 g (66%) 4-[N′-(2-fluorophenyl)ureido]-3-methoxyphenylacetic acid as a white crystalline powder. mp 185 –188 (d); 1H-NMR (DMSO-d6) δ 3.50 (2H, s), 3.82 (3H, s), 6.78 (1H, dd, J=1.4 and 8.3 Hz), 6.92 (1H, d, J=1.4 Hz), 6.95–7.01 (1H, m), 7.10–7.14 (1H, m), 7.19–7.24 (1H, m), 8.01 (1H, d, J=8.3 Hz), 8.14–8.18 (1H, m), 8.72 (1H, s), 9.17 (1H, s); MS (FAB) m/z 319 (M++1); Anal. Calcd for C16H15N2O4F: C, 60.37; H, 4.75; N, 8.80. Found: C, 60.20; H, 4.82; N, 8.67.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179819B2
Source datasetuspto-grants-2007_02
ORD IDord-46702510eac946d19b54101a37c9b0ef
Source noteuspto-grants-2007_02