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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693985Generated: October 31, 2026

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

https://huagongshe.com/reaction/1693985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactantdimethylsulfoxide THFHCID 21830753—
Reactant4-(2-Furan-2-yl-ethyl)-((E)-2-nitro-vinyl)-benzeneHCID 59255163—
SolventWaterHCID 962—
Product4-(2-Furan-2-yl-ethyl)-(2-nitro-ethyl)-benzeneHCID 5925551653.6%

Reaction Steps

To a mixed tetrahydrofuran-dimethyl sulfoxide (1:1, 10 mL) solution of 4-(2-furan-2-yl-ethyl)-((E)-2-nitro-vinyl)-benzene (554 mg, 2.28 mmol) described in Manufacturing Example 80-1-5 and acetic acid (0.5 mL) was added sodium borohydride (129 mg, 3.42 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 10 minutes at room temperature. Water was added dropwise into this reaction solution 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 (t-butylmethyl ether:heptane=5:95) to obtain the title compound (300 mg, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-33b1335bfa684172816b219de6140c51
Source noteuspto-grants-2012_04