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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693873Generated: November 1, 2026

Acetic Acid → 2-(2-Nitro-ethyl)-5-p-tolyloxy-thiophene

https://huagongshe.com/reaction/1693873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium borohydrideHCID 4311764—
Reactant2-((E)-2-Nitro-vinyl)-5-p-tolyloxy-thiopheneHCID 59255446—
SolventWaterHCID 962—
Product2-(2-Nitro-ethyl)-5-p-tolyloxy-thiopheneHCID 5925534247.6%

Reaction Steps

To a dimethyl sulfoxide (30.0 mL) solution of 2-((E)-2-nitro-vinyl)-5-p-tolyloxy-thiophene (2.50 g, 9.57 mmol) described in Manufacturing Example 48-1-3 and acetic acid (2.50 mL) was added sodium borohydride (610 mg, 20.6 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 30 minutes at room temperature. Water was then added dropwise at room temperature while cooling appropriately. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure and the residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:4) to obtain the title compound (1.20 g, 47.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-209f6a0367d34608b5cfaf2e7f66b22f
Source noteuspto-grants-2012_04