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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78064Generated: October 28, 2026

Acetic Acid → 2-(4-Methyl-benzyl)-5-(2-nitro-ethyl)-thiophene

https://huagongshe.com/reaction/78064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(4-Methyl-benzyl)-5-((E)-2-nitro-vinyl)-thiopheneHCID 59255318—
SolventWaterHCID 962—
Product2-(4-Methyl-benzyl)-5-(2-nitro-ethyl)-thiopheneHCID 5925546043.4%

Reaction Steps

To a dimethyl sulfoxide (20.0 mL) solution of 2-(4-methyl-benzyl)-5-((E)-2-nitro-vinyl)-thiophene (1.20 g, 4.63 mmol) described in Manufacturing Example 92-1-3 and acetic acid (1.20 mL) was added sodium borohydride (280 mg, 7.41 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 20 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 crystallized with a tetrahydrofuran-ethyl acetate-heptane system and filtered to obtain the title compound (525 mg, 43.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-b83938ae7eb6481cbec41d83efef3be6
Source noteuspto-grants-2014_09