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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78069Generated: October 26, 2026

Acetic Acid → 4-(2-Pyridin-2-yl-ethyl)-(2-nitro-ethyl)-benzene

https://huagongshe.com/reaction/78069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactantdimethylsulfoxide THFHCID 21830753—
Reactant4-(2-Pyridin-2-yl-ethyl)-((E)-2-nitrovinyl)-benzeneHCID 59255360—
SolventWaterHCID 962—
Product4-(2-Pyridin-2-yl-ethyl)-(2-nitro-ethyl)-benzeneHCID 5925531974.2%

Reaction Steps

To a mixed tetrahydrofuran-dimethyl sulfoxide (1:1) solution of 4-(2-pyridin-2-yl-ethyl)-((E)-2-nitro-vinyl)-benzene (2.83 g, 11.1 mmol) described in Manufacturing Example 93-1-6 and acetic acid (3 mL) was added sodium borohydride (630 mg, 16.7 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 15 minutes at room temperature. Water was added dropwise into this reaction mixture at room temperature while cooling appropriately. The reaction mixture was partitioned into water and ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate: heptane=1:9 then 2:8) to obtain the title compound (2.11 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-371aefb0737d42c58ccce35bad175d94
Source noteuspto-grants-2014_09