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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640335Generated: October 29, 2026

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

https://huagongshe.com/reaction/640335

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 numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-48924b3b2cc249f3b9c5d5654c7c32e5
Source noteuspto-grants-2010_04