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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269601Generated: October 30, 2026

1,2-Dichloroethane → HCID 131721923, compound

https://huagongshe.com/reaction/2269601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHydrochloric AcidHCID 313—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 57194832HCID 57194832—
ReactantHCID 131721921HCID 131721921—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 131721923HCID 13172192385%

Reaction Conditions

Temperature0 °C

Reaction Steps

Boc-Gly-Nleu-OH (12.5 g, 0.043 mol.), HCl.Pro-OBz (11 g, 0.046 mol.) and HOBt (6.0 g, 0.045 mol.) were dissolved in 300 ml DMF and the solution was chilled to 0° C. Triethylamine (12 ml) was added slowly while stirring the solution. After 5 minutes, EDC (8.5 g, 0.043 mol.) was added to the solution and the stirring was continued at room temperature overnight. The DMF was removed under reduced pressure and the resulting mixture was poured into 350 ml ethyl acetate. The ethyl acetate solution was washed by H2O, saturated NaHCO3, brine, saturated NaHSO4 and brine again until the pH of the brine layer was about 7. The organic layer was dried by Na2SO4 and the ethyl acetate was removed under reduced pressure to get the crude product. Column chromatography (elution solvents: E/H, 3:1) was carried out to obtain the pure product (17.5 g, 85%). TLC Rf=0.45 (developing solvents: E/H, 3:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329506B1
Source datasetuspto-grants-2001_12
ORD IDord-6d2fff9ec1c844c88230cb5dd86588a5
Source noteuspto-grants-2001_12