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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640201Generated: October 28, 2026

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

https://huagongshe.com/reaction/640201

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 numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-b216c52bef9b40978601323364af8602
Source noteuspto-grants-2010_04