Acetone imine

Acetone imine, or 2-propanimine is an organic compound and an imine with the chemical formula (CH3)2CNH. It is a volatile and flammable liquid at room temperature. It is the simplest ketimine. This compound is mainly of academic interest.

Acetone imine
Full structural formula of acetone imine with dimensions
Skeletal formula of acetone imine
Ball-and-stick model of acetone imine
Space-filling model of acetone imine
Names
Preferred IUPAC name
2-Propanimine
Systematic IUPAC name
Propan-2-imine[1]
Other names
  • acetone imine
Identifiers
ChemSpider
MeSH Imine Acetone Imine
Properties
C3H7N
Molar mass 57.096 g·mol−1
Appearance colorless liquid
Density 0.8 g cm−3 (25 °C)
Boiling point 57–59 °C (135–138 °F; 330–332 K)
log P -0.56
1.394
Hazards
GHS pictograms
GHS Signal word Danger
GHS hazard statements
 H225, H319, H336
P210, P261, P305+351+338
NFPA 704 (fire diamond)
Flammability code 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineHealth code 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazard W: Reacts with water in an unusual or dangerous manner. E.g. sodium, sulfuric acid
3
0
0
Flash point 14.7 °C (58.5 °F; 287.8 K)
Related compounds
Related compounds
 Acetone oxime
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Synthesis and reactions

Acetone imine is prepared by dehydrocyanation of the cyanoamine of acetone, which is prepared from acetone cyanohydrin. Dicyclohexylcarbodiimide (CyN=C=NCy) serves as the scavenger for hydrogen cyanide:[2]

(CH3)2C(NH2)CN + CyN=C=NCy → (CH3)2CNH + CyN(H)-C(CN)=NCy
Upon standing at room temperature, samples of acetone imine degrade to give this heterocycle, called acetonin.

The compound hydrolyzes readily:

(CH3)2CNH + H2O → (CH3)2CO + NH3

This reactivity is characteristic of imines derived from ammonia. Methylene imine (CH2=NH) is also highly reactive, condensing to hexamethylenetetramine. Upon standing, the imine undergoes further condensation to give the tetrahydropyrimidine called acetonin, with loss of ammonia.[3]

The imine of hexafluoroacetone, ((CF3)2C=NH) is by contrast robust.[4]

gollark: This occurs in the final phase of potatoBIOS initialization:```luaif potatOS.registry.get "potatOS.immutable_global_scope" then setmetatable(_G, { __newindex = function(_, x) error(("cannot set _G[%q] - _G is immutable"):format(tostring(x)), 0) end })endif meta then _G.meta = meta.new() endif _G.textutilsprompt then textutils.prompt = _G.textutilsprompt endif process then process.spawn(keyboard_shortcuts, "kbsd") if http.websocket then process.spawn(skynet.listen, "skynetd") process.spawn(potatoNET, "systemd-potatod") end local autorun = potatOS.registry.get "potatOS.autorun" if type(autorun) == "string" then autorun = load(autorun) end if type(autorun) == "function" then process.spawn(autorun, "autorun") end if potatOS.registry.get "potatOS.extended_monitoring" then process.spawn(excessive_monitoring, "extended_monitoring") end if run then process.spawn(run_shell, "ushell") endelse if run then print "Warning: no process manager available. This should probably not happen - please consider reinstalling or updating. Fallback mode enabled." local ok, err = pcall(run_shell) if err then printError(err) end os.shutdown() endendwhile true do coroutine.yield() end```
gollark: (this applies after all the legacy `os.loadAPI` stuff loads anyway)
gollark: Too bad.
gollark: I would apply this to the various `_ENV`s, except that probably would break shell.
gollark: I *could* have a "strict" option where it makes all the tables immutable too, I suppose.

References
  1. "Synonyms". Pubchem.
  2. K. Findeisen; H. Heitzer; K. Dehnicke (1981). "Neue Methode zur Herstellung von Aldiminen und Ketiminen". Synthesis: 702–704. doi:10.1055/s-1981-29566.
  3. Matter, E. (1947). "Über ein neues Reaktionsprodukt aus Aceton und Ammoniak (Acetonin) (A new reaction product from acetone and ammonia (acetonine)) I". Helvetica Chimica Acta. 30: 1114–23. doi:10.1002/hlca.19470300503.
  4. W. J. Middleton, H. D. Carlson (1970). "Hexafluoroacetone imine". Org. Syntheses. 50: 81–3. doi:10.15227/orgsyn.050.0081..
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