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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840868Generated: November 1, 2026

1,2-Dichloroethane → HCID 15885812, compound

https://huagongshe.com/reaction/1840868

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
ReactantHCID 15885811HCID 15885811—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 15885812HCID 1588581255.3%

Reaction Steps

To a stirred solution of 2-(3-ethylureido)-6-methylbenzoic acid (250 mg, 1.125 mmol) and triethylamine (170 mg, 1.69 mmol) in 10 mL CH2Cl2 at room temperature was added EDC (501 mg, 1.69 mmol). After stirring at room temperature for 3 hours, the reaction mixture was diluted with EtOAc and washed sequentially with 1N HCl and sat'd. NaHCO3. The organic fraction was dried (MgSO4), filtered and evaporated under reduced pressure. Silica gel chromatography of the residue (1:1 EtOAc/hexane) afforded 127 mg of product: Anal. Calc'd. for C11H12N2O2.0.25H2O: C, 63.30; H, 6.04; N, 13.42. Found: C, 63.32; H, 5.92; N, 13.10. 1H-NMR (300 MHz, d6-DMSO) δ 1.14 (t, J=7 Hz, 3H), 2.60 (s, 3H), 3.27 (pent, J=7 Hz, 2H), 6.95 (d, J=8 Hz, 1H), 7.02 (d, J=8 Hz, 1H), 7.50 (t, J=8 Hz, 1H), 7.90 (br. t, J=7 Hz, 1H, exchangeable).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683077B2
Source datasetuspto-grants-2004_01
ORD IDord-0709f946d6e04968868385451de9fb6a
Source noteuspto-grants-2004_01