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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260201Generated: October 30, 2026

1,2-Dichloroethane → HCID 54591523, compound

https://huagongshe.com/reaction/1260201

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantN,N-DimethylglycineHCID 673—
ReactantHCID 54591302HCID 54591302—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 54591523HCID 5459152350.4%

Reaction Steps

86 mg (0.70 mmol) of 4-N,N-dimethylaminopyridine and 671 mg (3.50 mmol) of EDC were added to a solution of 550 mg (1.17 mmol) of the compound from Example 1 and 361 mg (3.50 mmol) of N,N-dimethylglycine in 11 ml of dichloromethane. After the reaction mixture had been stirred at RT for 8 h, all volatile constituents were removed on a rotary evaporator. The residue obtained was taken up in 200 ml of ethyl acetate and washed once with approx. 100 ml of water. After drying over anhydrous magnesium sulphate, filtration and concentration, the product was isolated by means of MPLC (approx. 30 g of silica gel, eluent: 25:25:1 cyclohexane/ethyl acetate/triethylamine) A first fraction of 328 mg of the title compound was obtained. A further 115 mg of the title compound were obtained from a second, still-contaminated fraction by recrystallization from cyclopentyl methyl ether. A total of 443 mg (68% of theory) of the title compound was thus obtained. Another crystallization from diisopropyl ether/cyclopentyl methyl ether (2:1, 1.5 ml per 100 mg) gave the title compound with a melting point of 117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470811B2
Source datasetuspto-grants-2013_06
ORD IDord-55a706e153b442b4979bc9dc79e6420a
Source noteuspto-grants-2013_06