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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956690Generated: November 3, 2026

1,2-Dichloroethane → HCID 19611597, compound

https://huagongshe.com/reaction/1956690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthyl AcetateHCID 8857—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-[(5-Formylimidazol-1-yl)methyl]benzonitrileHCID 10632289—
ProductHCID 19611597HCID 19611597—

Reaction Conditions

Temperature0 °C

Reaction Steps

The amine hydrochloride from Step A (978 mg) was partitioned between dilute aqueous NaHCO3 solution and methylene chloride. The aqueous layer was washed with three portions of CH2Cl2, and the combined organics were dried (Na2SO4), filtered, and concentrated in vacuo to provide the free amine. To a solution of the amine in 11 mL of 1,2-dichloroethane at 0° C. was added 4 Å powdered molecular sieves (2 g), followed by sodium triacetoxyborohydride (3.04 g). The aldehyde from Step E of Example 1 (1.21 g) was added, and the reaction was stirred at 0° C. After 15 hours, , the reaction was poured into EtOAc, washed with sat. aq. NaHCO3, and the aqueous layer was extracted with EtOAc. The combined organics were washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo. The resulting product was taken up in 60 mL of 5:1 benzene:CH2Cl2, and propylamine (10 mL) was added. The reaction was stirred for 12 hours, then concentrated in vacuo, and purified by silica gel chromatography (5% MeOH/CHCl3) to provide the titled compound (1.33 g) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780492
Source datasetuspto-grants-1998_07
ORD IDord-31b6572f49914c6383732b6714027735
Source noteuspto-grants-1998_07