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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691024Generated: October 30, 2026

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

https://huagongshe.com/reaction/1691024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantNitromethaneHCID 6375—
ReactantAmmonium AcetateHCID 517165—
Reactant5-p-Tolyloxy-thiophene-2-carbaldehydeHCID 59255412—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-((E)-2-Nitro-vinyl)-5-p-tolyloxy-thiopheneHCID 5925544691.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

To an acetic acid (20.0 mL) solution of 5-p-tolyloxy-thiophene-2-carbaldehyde (2.30 g, 10.5 mmol) described in Manufacturing Example 48-1-2 were added nitromethane (3.20 g, 52.5 mmol) and ammonium acetate (1.62 g, 21.0 mmol) under nitrogen atmosphere at room temperature, which was stirred for 2.5 hours at 100° C. Water and ethyl acetate were added to the reaction mixture, and the organic layer was extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The solvent was evaporated from the filtrate under a reduced pressure to obtain the title compound (2.50 g) as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-66337c5511d840d5b9c8e377ecc8c131
Source noteuspto-grants-2012_04