HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77917Generated: October 29, 2026
Acetic Acid → 2-((E)-2-Nitro-vinyl)-5-p-tolyloxy-thiophene
https://huagongshe.com/reaction/77917
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 5-p-Tolyloxy-thiophene-2-carbaldehyde | HCID 59255412 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-((E)-2-Nitro-vinyl)-5-p-tolyloxy-thiophene | HCID 59255446 | 91.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841327B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-02bfc601ac9043c0bc4376463aa0b131 |
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| Source note | uspto-grants-2014_09 |
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