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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945382Generated: November 1, 2026

1,2-Dichloroethane → HCID 797770, compound

https://huagongshe.com/reaction/1945382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant(4-Nitrophenoxy)acetic acidHCID 15720—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzoic acid, 3-amino-, methyl esterHCID 78274—
ReactantDiisopropylethylamineHCID 81531—
SolventDimethylformamideHCID 6228—
ProductHCID 797770HCID 79777090.8%

Reaction Steps

To a solution of the 4-nitrophenoxy acetic acid (100 mg, 0.5 mmol), 3-amino benzoic acid methyl ester (115 mg, 0.76 mmol), HOBt (102.81 mg, 0.76 mmol) and DIPEA (98.34 mg, 0.76 mmol) in DMF (4.0 mL) were added EDC (145.86 mg, 0.76 mmol) at room temperature. After reaction terminated, the reaction mixture in cool water was diluted with Ethyl acetate. The organic phase was washed with aqueous sodium bicarbonate and dried (anhydrous MgSO4), and concentrated. Purification by silica gel column chromatography (Ethyl acetate:Hexane=1:9˜1:1) gave 3-[2-(4-nitro-phenoxy)acetyl-amino]-benzoic acid methyl ester as a white solid (150 mg, 89% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394799B2
Source datasetuspto-grants-2013_03
ORD IDord-a895fcc91a254a9f971245af41382fbd
Source noteuspto-grants-2013_03