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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78052Generated: October 28, 2026

Acetic Acid → 1-(2-Nitro-ethyl)-4-phenoxymethyl-benzene

https://huagongshe.com/reaction/78052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactant1-((E)-2-Nitro-vinyl)-4-phenoxymethyl-benzeneHCID 59255212—
SolventDimethyl SulfoxideHCID 679—
Product1-(2-Nitro-ethyl)-4-phenoxymethyl-benzeneHCID 5925545751%

Reaction Steps

To an acetic acid (4.1 mL) and dimethyl sulfoxide (70 mL) solution of 1-((E)-2-nitro-vinyl)-4-phenoxymethyl-benzene (4.1 g, 16.2 mmol) described in Manufacturing Example 86-1-3 was added sodium borohydride (981 mg, 25.9 mmol) at room temperature while cooling appropriately. This mixture was stirred for 1 hour at room temperature. The mixture was partitioned into ethyl acetate and water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=4:1) to obtain the title compound (2.11 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-1406e6ac21514bc4a56da379e84dd83a
Source noteuspto-grants-2014_09