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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426880Generated: October 30, 2026

2-Nitrobenzaldehyde → HCID 5170752, compound

https://huagongshe.com/reaction/426880

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrobenzaldehydeHCID 11101—
ReactantCyclopropyl methyl ketoneHCID 13004—
ProductHCID 5170752HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04171378
Source datasetuspto-grants-1979_10
ORD IDord-80da58a6c1044de4a1c1bf1206efc95e
Source noteuspto-grants-1979_10