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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787946Generated: October 29, 2026

1,2-Dichloroethane → HCID 57602578, compound

https://huagongshe.com/reaction/1787946

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactanttert-Butyl (4-aminobut-2-yn-1-yl)carbamateHCID 16005182—
ReactantHCID 22324246HCID 22324246—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 57602578HCID 5760257872%

Reaction Steps

To a solution of (4-Amino-but-2-ynyl)-carbamic acid tert-butyl ester (0.8 g, 4.34 mmol) in dry CH2Cl2 (40 ml) was added 6,6-bis-(4-fluorophenyl)-hexanoic acid (1.32 g, 4.4 mmol) under nitrogen. To the reaction was added EDC (1.66 g, 8.68 mmol) and DMAP (cat) and the reaction mixture stirred under nitrogen at room temperature overnight. The reaction was then concentrated under reduced pressure. The residue dissolved in ethyl acetate: water (10:1) (150 ml). The organic was washed with water (30 ml, 2×) and 10% NaOH (30 ml) and dried over MgSO4 and evaporated to dryness. The resulting residue was purified by column chromatography using CH2Cl2:CH3OH (15:1) to give the desired product in 72% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511077B2
Source datasetuspto-grants-2009_03
ORD IDord-f7e815d18ea74850b93ae3550c8d918f
Source noteuspto-grants-2009_03