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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691144Generated: November 2, 2026

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

https://huagongshe.com/reaction/1691144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactantdimethylsulfoxide THFHCID 21830753—
Reactant4-(2-(Tetrahydrofuran-2-yl)-ethyl)-((E)-2-nitro-vinyl)benzeneHCID 59255150—
SolventWaterHCID 962—
Product4-(2-(Tetrahydrofuran-2-yl)-ethyl)-(2-nitro-ethyl)-benzeneHCID 5925529965%

Reaction Steps

To a mixed tetrahydrofuran-dimethyl sulfoxide (1:1, 10 mL) solution of 4-(2-(tetrahydrofuran-2-yl)-ethyl)-((E)-2-nitro-vinyl)-benzene (646 mg, 2.61 mmol) described in Manufacturing Example 82-1-4 and acetic acid (0.6 mL) was added sodium borohydride (148 mg, 3.92 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 10 minutes at room temperature. Water was added dropwise into the 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=2:8) to obtain the title compound (421 mg, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-2823c83908e74dc6802b1fa880a32b22
Source noteuspto-grants-2012_04