2-Nitrocinnamaldehyde

2-Nitrocinnamaldehyde, ortho-nitrocinnamaldehyde or o-nitrocinnamaldehyde is an organic aromatic compound containing a nitro group ortho- to the 1-position of cinnamaldehyde.

2-Nitrocinnamaldehyde[1]
Names
IUPAC name
(E)-3-(2-Nitrophenyl)prop-2-enal
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
Properties
C9H7O3N
Appearance Pale yellow crystalline powder
Melting point 124 to 126 °C (255 to 259 °F; 397 to 399 K)
Slightly soluble
Hazards
S-phrases (outdated) S24 S25
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Synthesis

2-Nitrocinnamaldehyde can be synthesized by dissolving cinnamaldehyde to a solution of acetic anhydride in acetic acid, and adding a stoichiometric amount of concentrated nitric acid at 0–5 °C. Yields are around 36-46% of theoretical.

Nitration of cinnamaldehyde via acidification of a nitrate salt with H2SO4 also yields the ortho-nitro compound, however it also yields some of the para-nitro compound, which is generally undesired.

2-Nitrocinnamaldehyde can also be prepared by reacting 2-nitrobenzaldehyde with acetaldehyde in a condensation reaction.[2]

Uses

2-Nitrocinnamaldehyde can be oxidized to 2-nitrocinnamic acid which can be used in the Baeyer-Emmerling indole synthesis to produce indole and substituted indoles.

gollark: You can try it in an emulator.
gollark: PotatOS is serious. But also for CC.
gollark: Obviously it can only detect virii and bad programs I know of and program in right now.
gollark: Also, it doesn't strictly filter code on *startup*, it filters *any code executed after bootup*.
gollark: [REDACTED], and [LEVEL Δ-7 CLEARANCE REQUIRED].

References

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.