''N'',''N''-Diisopropylethylamine

N,N-Diisopropylethylamine
Names
Preferred IUPAC name
N-Ethyl-N-(propan-2-yl)propan-2-amine
Other names
  • Ethyldi(propan-2-yl)amine
  • N-ethyl-N-isopropylpropan-2-amine
  • Ethyldi(isopropyl)amine
  • Hünig's base
  • DIPEA
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.027.629
EC Number 230-392-0
MeSH N,N-diisopropylethylamine
UN number 2733
Properties
C8H19N
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)
1.414
Hazards
GHS pictograms
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).
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Infobox references

N,N-Diisopropylethylamine, or Hünig's base, is an organic compound and an amine. It is named after the German chemist Siegfried Hünig. It is used in organic chemistry as a base. It is commonly abbreviated as DIPEA, DIEA, or i-Pr2NEt.

Structure

DIPEA consists of a central nitrogen that is bonded to an ethyl group and two isopropyl groups. A lone pair of electrons resides on the nitrogen atom, which can react with electrophiles. However, as the two isopropyl groups and the ethyl group occupy much of the space surrounding the nitrogen, only small electrophiles such as protons can react with the nitrogen lone pair.

Occurrence and preparation

DIPEA is synthetically produced and commercially available. It is traditionally prepared by the alkylation of diisopropylamine with diethyl sulfate.[1]

Pure DIPEA exists as a colorless liquid, although commercial samples can be slightly yellow. If necessary, the compound can be purified by distillation from potassium hydroxide[2] or calcium hydride.[3]

Uses and reactions

DIPEA is a hindered base that is commonly employed as an acid or proton scavenger. Thus, like 2,2,6,6-tetramethylpiperidine and triethylamine, DIPEA is a good base but a poor nucleophile, a combination of properties that makes it a useful organic reagent.[4]

Amide coupling

It is commonly used as the hindered base in amide coupling reactions between a carboxylic acid (typically activated, for example, as an acid chloride, as illustrated below) and a nucleophilic amine.[5] As DIPEA is hindered and poorly nucleophilic, it does not compete with the nucleophilic amine in the coupling reaction.

Alkylations

DIPEA has been investigated for its use as a selective reagent in the alkylation of secondary amines to tertiary amines by alkyl halides. This is often hampered by an unwanted Menshutkin reaction forming a quaternary ammonium salt but this side-reaction is absent when DIPEA is present.[6]

Transition metal catalyzed cross-coupling reactions

DIPEA can be used as a base in a number of transition metal catalyzed cross-coupling reactions, such as the Heck coupling and the Sonogashira coupling (as illustrated below).[7]

Swern oxidation

Although triethylamine is traditionally employed as the hindered base in Swern oxidations, the structurally similar DIPEA can be used instead, as exemplified below.[8]

Examples of DIPEA used as a substrate

DIPEA forms a complex heterocyclic compound called scorpionine (bis([1,2]dithiolo)-[1,4]thiazine) by a reaction with disulfur dichloride catalyzed by DABCO in a one-pot synthesis.[9]

Comparison with triethylamine

DIPEA and triethylamine are structurally very similar, with both compounds considered hindered organic bases. Due to their structural similarity, DIPEA and triethylamine can be used interchangeably in most applications. The nitrogen atom in DIPEA is more shielded than the nitrogen atom in triethylamine. However, triethylamine is a slightly stronger base than DIPEA; the pKas of the respective conjugate acids in dimethyl sulfoxide are 9.0 and 8.5, respectively.[10]

References

  1. ↑ Hünig, S.; Kiessel, M. (1958). "Spezifische Protonenacceptoren als Hilfsbasen bei Alkylierungs- und Dehydrohalogenierungsreaktionen". Chemische Berichte. 91 (2): 380–392. doi:10.1002/cber.19580910223.
  2. ↑ Armarego, W. L. F. Purification of Laboratory Chemicals. Chai, Christina Li Lin, (Seventh ed.). Amsterdam. ISBN 9780123821621. OCLC 820853648.
  3. ↑ Keiper, Sonja; Vyle, Joseph S. (2006-05-12). "Reversible Photocontrol of Deoxyribozyme-Catalyzed RNA Cleavage under Multiple-Turnover Conditions". Angewandte Chemie International Edition. 45 (20): 3306–3309. doi:10.1002/anie.200600164. ISSN 1433-7851.
  4. ↑ Sorgi, K. L. (2001). "Diisopropylethylamine". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rd254.
  5. ↑ Dunetz, Joshua R.; Magano, Javier; Weisenburger, Gerald A. (2016-02-05). "Large-Scale Applications of Amide Coupling Reagents for the Synthesis of Pharmaceuticals". Organic Process Research & Development. 20 (2): 140–177. doi:10.1021/op500305s. ISSN 1083-6160.
  6. ↑ 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.
  7. ↑ Chinchilla, Rafael; Nájera, Carmen (2011). "Recent advances in Sonogashira reactions". Chemical Society Reviews. 40 (10): 5084. doi:10.1039/c1cs15071e. ISSN 0306-0012.
  8. ↑ Walba, David M.; Thurmes, William N.; Haltiwanger, R. Curtis (1988). "A highly stereocontrolled route to the monensin spiroketal ring system". The Journal of Organic Chemistry. 53 (5): 1046–1056. doi:10.1021/jo00240a022. ISSN 0022-3263.
  9. ↑ 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.
  10. ↑ Lepore, Salvatore D.; Khoram, Anita; Bromfield, Deborah C.; Cohn, Pamela; Jairaj, Vinod; Silvestri, Maximilian A. (2005). "Studies on the Manganese-Mediated Isomerization of Alkynyl Carbonyls to Allenyl Carbonyls". The Journal of Organic Chemistry. 70 (18): 7443–7446. doi:10.1021/jo051040u. ISSN 0022-3263.
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