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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916632Generated: October 28, 2026

1,2-Dichloroethane → HCID 22350153, compound

https://huagongshe.com/reaction/916632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAcetic AcidHCID 176—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-[1-(Benzenesulfonyl)indol-4-yl]oxyethanamineHCID 10267837—
ProductHCID 22350153HCID 22350153—

Reaction Steps

A mixture of 2-{[1-(phenylsulfonyl)-1H-indole-4-yl]oxy}ethylamine (0.316 g, 1.0 mmol), tetrahydro-4H-pyran-4-one (0.09 ml, 1.00 mmol) and sodium triacetoxyborohydride (0.312 g, 1.4 mmol) in 1,2-dichloroethane is treated with acetic acid (0.06 ml) at room temperature, stirred under nitrogen for 18 hr, quenched with concentrated aqueous NH4OH and diluted with methylene chloride and water. The aqueous layer is separated and extracted with methylene chloride. The organic layer and extracts are combined, washed with saturated NaCl, dried over Na2SO4, and concentrated in vacuo. The resultant residue is purified by flash chromatography (silica gel, EtOAc/MeOH/NH4OH: 9/1/0.05) to afford the free amine of the title product as a clear oil, 0.36 g (90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271180B2
Source datasetuspto-grants-2007_09
ORD IDord-f2f1c04d818340b48129ace02a551bd6
Source noteuspto-grants-2007_09