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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322083Generated: October 30, 2026

1,2-Dichloroethane → HCID 15521926, compound

https://huagongshe.com/reaction/322083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
ReactantSodium HydroxideHCID 14798—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantHCID 69710510HCID 69710510—
SolventEthanolHCID 702—
SolventAcetonitrileHCID 6342—
ProductHCID 15521926HCID 15521926—

Reaction Steps

To a solution of 4-8 (5.6 g, 12.8 mmol) in ethanol (50 mL) was added NaOH (15 mL 1M solution in water, 15 mmol). After stirring for 1 h, HCl (15 mL 1M solution in water, 15 mmol) was added, and the mixture evaporated to give an oily residue. The residue was evaporated from ethanol three times, and then from acetonitrile three times, producing a yellow crusty solid which was dried under a vacuum of <2 mm Hg for 2 h. This residue was then slurried in chloroform (5 mL) and acetonitrile (50 mL), and NMM (8.5 mL), N,O-dimethylhydroxylamine hydrochloride (2.5 g, 26 mmol), HOBT (1.7 g, 13 mmol) and EDC (2.4 g, 13 mmol) were added. After stirring for 15 h, the mixture was evaporated to dryness, the residue slurried in EtOAc, washed with sat. NaHCO3, brine, and dried over Na2SO4. Evaporative removal of the solvent gave 4-9 as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211191B1
Source datasetuspto-grants-2001_04
ORD IDord-f5f1de93df4949fc88dd1c76af276a0b
Source noteuspto-grants-2001_04