HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426880Generated: October 30, 2026
2-Nitrobenzaldehyde → HCID 5170752, compound
https://huagongshe.com/reaction/426880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | Cyclopropyl methyl ketone | HCID 13004 | — |
| Product | HCID 5170752 | HCID 5170752 | — |
Reaction Steps
2-Nitrobenzaldehyde is condensed with methyl cyclopropyl ketone to give 2-(2-nitrophenyl)vinyl cyclopropyl ketone. The latter is reduced selectively with hydroxylamine and hydroxylamine O-sulfonic acid in dilute sodium hydroxide solution to yield 2-(2-nitrophenyl)ethyl cyclopropyl ketone, which is then reduced with sodium borohydride to 2-(2-nitrophenyl)ethyl cyclopropyl carbinol. The carbinol is treated in the usual way with phosphorus tribromide and zinc bromide to afford 4-[6-(2-nitrophenyl)-3-hexenyl] bromide. The latter is reacted with potassium iodide, potassium carbonate and 3,5-heptanedione to produce 4-[6-(2-nitrophenyl)-3-hexenyl]-3,5-heptanedione which is selectively reduced with hydroxylamine and hydroxylamine O-sulfonic acid to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04171378 |
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| Source dataset | uspto-grants-1979_10 |
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| ORD ID | ord-80da58a6c1044de4a1c1bf1206efc95e |
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| Source note | uspto-grants-1979_10 |
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