HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78241Generated: October 25, 2026
Acetic Acid → trans-4-Bromo-beta-nitrostyrene
https://huagongshe.com/reaction/78241
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Water | HCID 962 | — |
| Product | trans-4-Bromo-beta-nitrostyrene | HCID 688204 | 83.8% |
Reaction Steps
A mixture of 4-bromobenzaldehyde (16.8 g, 91 mmol), nitromethane (24.6 mL, 455 mmol), ammonium acetate (14 g, 182 mmol), and acetic acid (160 mL) was stirred for 4 hours at 100° C. This mixture was cooled to room temperature and poured into water. The precipitate thus produced was collected, washed with water, and dried under a reduced pressure to obtain the title compound (17.4 g). 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-047d50064f2148ab898bc3dc70987e87 |
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| Source note | uspto-grants-2014_09 |
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