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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691089Generated: November 1, 2026

Acetic Acid → (4-(2-Nitro-ethyl)-phenyl)-phenyl-amine

https://huagongshe.com/reaction/1691089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactant(4-((E)-2-nitro-vinyl)-phenyl)-phenyl-amineHCID 59255421—
SolventDimethyl SulfoxideHCID 679—
Product(4-(2-Nitro-ethyl)-phenyl)-phenyl-amineHCID 2391317762%

Reaction Steps

To an acetic acid (3.2 mL) and dimethyl sulfoxide (54 mL) solution of (4-((E)-2-nitro-vinyl)-phenyl)-phenyl-amine (3.2 g, 13.4 mmol) described in Manufacturing Example 69-1-2 was added sodium borohydride (811 mg, 21.4 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=4:1-2:1) to obtain the title compound (2.01 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-deb689d5486941dc914d38f81072b3b3
Source noteuspto-grants-2012_04