HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78234Generated: October 30, 2026
Nitromethane → 1-Benzylsulfanyl-4-((E)-2-nitro-vinyl)-benzene
https://huagongshe.com/reaction/78234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 4-(Benzylsulfanyl)benzaldehyde | HCID 12842460 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-Benzylsulfanyl-4-((E)-2-nitro-vinyl)-benzene | HCID 59255337 | 95.1% |
Reaction Steps
A mixture of 4-benzylsulfanyl-benzaldehyde (840 mg 3.68 mmol) described in Manufacturing Example 205-1-2, nitromethane (997 μL, 18.4 mmol), ammonium acetate (567 mg, 7.36 mmol), and acetic acid (10 mL) was stirred for 2 hours at 100° C. This mixture was cooled to room temperature and concentrated under reduced pressure. The residue was partitioned into ethyl acetate and water. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (950 mg). The title compound was used in the following reaction without any further purification.
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-956403545c854a9eb677a76685d2ca92 |
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| Source note | uspto-grants-2014_09 |
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