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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352809Generated: October 30, 2026

1,2-Dichloroethane → Diethyl 5-[[(phenylmethoxy)amino]carbonyl]-1,3-benzenedicarboxylate

https://huagongshe.com/reaction/1352809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
Reactant3,5-Bis(ethoxycarbonyl)benzoateHCID 22575049—
ProductDiethyl 5-[[(phenylmethoxy)amino]carbonyl]-1,3-benzenedicarboxylateHCID 1201754458.9%

Reaction Steps

To a solution of diethyl 1,3,5-benzenetricarboxylate (3.192 g, 20 mol) and O-benzylhydroxyamine hydrochloride (4.789 g, 19 mmol) in 40 mL were added N-methylmorpholine (2.2 mL, 20 mmol) and EDC (3.834 g, 20 mmol) at 0° C., and the mixture was stirred at room temperature for 20 hours. The solvent was removed by evaporator and the residue was dissolved in EtOAc (150 mL). The organic solution was washed with 1 N HCL (150 mL), washed with saturated aqueous NaHCO3 (50 mL), dried over Na2SO4, and concentrated to give white solid. This material was recrystallized from EtOAc to give 4.154 g of white powder: 1H NMR (CDCl3) δ 1.41 (t, 6H), 4.40 (q, 4H), 5.05 (s, 2H), 7.3-7.5 (m, 5H), 8.52 (s, 2H), 8.76 (s, 1H), 9.1 (br, 1H). TLC: Rf 0.62 (EtOAc/Hexanes 1/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220780B2
Source datasetuspto-grants-2007_05
ORD IDord-7db6242a6e1e4d0f8bc2279e0de434c6
Source noteuspto-grants-2007_05