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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017680Generated: October 30, 2026

1,1-Dichloroethane → HCID 18403870, compound

https://huagongshe.com/reaction/1017680

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 18403741HCID 18403741—
ProductHCID 18403870HCID 1840387042.1%

Reaction Steps

To a solution of 4-benzyloxy-3-(ethoxycarbonylmethoxy)benzaldehyde (0.2 g) in dichloroethane (4 ml) was added (pyridin-2-yl)piperazine (0.12 ml) and sodiumtriacetoxy borohydride (0.25 g), with stirring. The reaction mixture was stirred at ambient temperature for 1.5 hrs, poured into ice/saturated sodium bicarbonate solution and extracted with ethyl acetate. The extracts were washed with water, saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was dissolved in dichloromethane and flash chromatographed (silica gel), eluting with dichloromethane, 1% and 2% methanol/dichloromethane. The appropriate fractions were collected and concentrated. The residue was dissolved in ether and ethereal hydrochloric acid was added. The suspension was filtered and the filter cake dried for 2 hrs at ambient temperature. Recrystallization from ethanol provided 0.143 g (42.1%) of product, mp 151-191° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479495B1
Source datasetuspto-grants-2002_11
ORD IDord-24a81b5616ff4b9b807afda8b276b6ba
Source noteuspto-grants-2002_11