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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77794Generated: October 25, 2026

Acetic Acid → 1-Benzyloxy-4-(2-nitro-ethyl)-benzene

https://huagongshe.com/reaction/77794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium borohydrideHCID 4311764—
Reactant(E)-1-(Benzyloxy)-4-(2-nitrovinyl)benzeneHCID 5702926—
SolventWaterHCID 962—
Product1-Benzyloxy-4-(2-nitro-ethyl)-benzeneHCID 2472103770.8%

Reaction Steps

To a mixture of 1-benzyloxy-4-((E)-2-nitro-vinyl)-benzene (1.0 g, 3.9 mmol) described in Manufacturing Example 1-1-1, acetic acid (1 mL) and dimethyl sulfoxide (17 mL) was added sodium borohydride (250 mg, 6.3 mmol) at room temperature while cooling appropriately, and the reaction mixture was stirred for 40 minutes at room temperature. Water was added to the reaction mixture. The reaction mixture was partitioned into ethyl acetate and water. 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=1:3) to obtain the title compound (710 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-b36260e7afd04b67bd43f728912f48e6
Source noteuspto-grants-2014_09