From Wikipedia, the free encyclopedia
  (Redirected from Hunig's base)
Jump to: navigation, search
Skeletal formula of N,N-diisopropylethylamine
Preferred IUPAC name
Other names
  • Ethyldi(propan-2-yl)amine
  • N-ethyl-N-isopropylpropan-2-amine
  • Ethyldi(isopropyl)amine
  • Hünig's base
3D model (JSmol)
ECHA InfoCard 100.027.629
EC Number 230-392-0
MeSH N,N-diisopropylethylamine
UN number 2733
Molar mass 129.25 g·mol−1
Appearance Colorless liquid
Odor Fishy, ammoniacal
Density 0.742 g mL−1
Melting point −50 to −46 °C (−58 to −51 °F; 223 to 227 K)
Boiling point 126.6 °C; 259.8 °F; 399.7 K
4.01 g/L (at 20 °C)
Vapor pressure 4.1 kPa (at 37.70 °C)
GHS pictograms The flame pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) The corrosion pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) The skull-and-crossbones pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
GHS signal word DANGER
H225, H301, H314, H412
P210, P273, P280, P301+310, P305+351+338, P310
Flash point 10 °C (50 °F; 283 K)
Explosive limits 0.7–6.3%
Lethal dose or concentration (LD, LC):
200–500 mg kg−1 (oral, rat)
Related compounds
Related amines
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

N,N-Diisopropylethylamine, or Hünig's base, DIPEA or DIEA, is an organic compound and an amine. It is used in organic chemistry as a base. Because the nitrogen atom is shielded by the two isopropyl groups and an ethyl group only a proton is small enough to easily fit. Like 2,2,6,6-tetramethylpiperidine, this compound is a good base but a poor nucleophile, which makes it a useful organic reagent.[1] Hünig's base is named after the German chemist Siegfried Hünig. The compound is a colourless liquid.

Hünig's base is commercially available. It is traditionally prepared by the alkylation of diisopropylamine with diethyl sulfate.[2] If necessary, the compound can be purified by distillation from potassium hydroxide.


Non-nucleophilic base[edit]

Hünig's base was investigated for its use as a selective reagent in the alkylation of secondary amines to tertiary amines by alkyl halides. This organic reaction is often hampered by a quaternization reaction to the quaternary ammonium salt but this side-reaction is absent when Hünig's base is present.[3]

The use of Hünig's base for alkylating secondary amines

Synthesis of scorpionine[edit]

Hünig's base forms a complex heterocyclic compound called scorpionine by a reaction with disulfur dichloride catalyzed by DABCO in a one-pot synthesis.[4]

Hünig's base in the synthesis of sscorpionine


  1. ^ Sorgi, K. L. (2001). "Diisopropylethylamine". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rd254. 
  2. ^ Hünig, S.; Kiessel, M. (1958). "Spezifische Protonenacceptoren als Hilfsbasen bei Alkylierungs- und Dehydrohalogenierungsreaktionen". Chemische Berichte. 91 (2): 380–392. doi:10.1002/cber.19580910223. 
  3. ^ Moore, J. L.; Taylor, S. M.; Soloshonok, V. A. (2005). "An efficient and operationally convenient general synthesis of tertiary amines by direct alkylation of secondary amines with alkyl halides in the presence of Huenig’s base". Arkivoc. 2005 (part vi): 287–292. EJ-1549C. 
  4. ^ Rees, W.; Marcos, C. F.; Polo, C.; Torroba, T.; Rakitin O. A. (1997). "From Hünig's Base to Bis([1,2]dithiolo)-[1,4]thiazines in One Pot: The Fast Route to Highly Sulfurated Heterocycles". Angewandte Chemie International Edition. 36 (3): 281–283. doi:10.1002/anie.199702811.