''tert''-Butanesulfinamide

tert-Butanesulfinamide
Skeletal formula of tert-butanesulfinamide
Ball-and-stick model of tert-butanesulfinamide
Names
IUPAC name
2-Methyl-2-propanesulfinamide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.108.188
Properties
(CH3)3CS(O)NH2
Molar mass 121.20 g/mol
Appearance white to off-white crystalline solid
Melting point 102 to 105 °C (216 to 221 °F; 375 to 378 K)
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

tert-Butanesulfinamide is an organosulfur compound and a member of the class of sulfinamides. Both enantiomeric forms are commercially available and are relevant to the asymmetric synthesis of amines as a chiral ammonia equivalent.[1][2][3] This methodology was introduced in 1997 by Jonathan A. Ellman.[4]

Synthesis

Chiral tert-butanesulfinamide can be prepared by enantioselective oxidation of inexpensive di-tert-butyl disulfide to the thiosulfinate followed by disulfide bond cleavage by lithium amide. In the original scope the chiral ligand used together with vanadyl acetylacetonate was prepared by condensing a chiral aminoindanol with 3,5-di-tert-butyl salicylaldehyde.

tert-Butanesulfinamide synthesis

Amine synthesis

Condensation with ketones and aldehydes yield the corresponding N-tert-butanesulfinyl aldimines and ketimines. These intermediates are more resistant to hydrolysis than other imines but more reactive towards nucleophiles. A nucleophile adds diastereoselectively over the imine group in an electrophilic addition with the tert-butanesulfinyl group acting as a chiral auxiliary. This tert-butanesulfinyl group is also a protecting group. On addition of hydrochloric acid the tert-butanesulfinyl group is removed forming the chiral primary ammonium salt or amine (from aldehyde precursor) or the chiral secondary amine (ketone precursor).

tert-Butanesulfinamide chiral amine synthesis

Typical nucleophiles are Grignard reagents, organozinc compounds, organolithium compounds, and enolates.

Chiral sulfinimines as intermediates for the asymmetric synthesis of amines have also been developed by Franklin A. Davis.[5]

Applications

tert-Butanesulfinamide has been used as an auxiliary in an asymmetric synthesis of cetirizine (more potent than the racemic mixture of the drug) starting from p-chlorobenzaldehyde and phenylmagnesium bromide:[6]

Asymmetric cetirizine synthesis

References

  1. ↑ Ellman, J. A. (2003). "Applications of tert-butanesulfinamide in the asymmetric synthesis of amines". Pure and Applied Chemistry. 75: 39. doi:10.1351/pac200375010039.
  2. ↑ Robak, Maryann T.; Herbage, Melissa A.; Ellman, Jonathan A. (2010). "Synthesis and Applications oftert-Butanesulfinamide". Chemical Reviews. 110 (6): 100426091145060. doi:10.1021/cr900382t. PMID 20420386.
  3. ↑ Organic Syntheses, Vol. 82, p.157 (2005). Link
  4. ↑ Liu, Guangcheng; Cogan, Derek A.; Ellman, Jonathan A. (1997). "Catalytic Asymmetric Synthesis oftert-Butanesulfinamide. Application to the Asymmetric Synthesis of Amines". Journal of the American Chemical Society. 119 (41): 9913. doi:10.1021/ja972012z.
  5. ↑ Davis, Franklin A.; Reddy, Rajarathnam E.; Szewczyk, Joanna M.; Reddy, G. Venkat; Portonovo, Padma S.; Zhang, Huiming; Fanelli, Dean; Zhou, Ping; et al. (1997). "Asymmetric Synthesis and Properties of Sulfinimines (ThiooximeS-Oxides)". The Journal of Organic Chemistry. 62 (8): 2555–2563. doi:10.1021/jo970077e. PMID 11671597.
  6. ↑ Pflum, D; Krishnamurthy, D; Han, Z; Wald, S; Senanayake, C (2002). "Asymmetric synthesis of cetirizine dihydrochloride". Tetrahedron Letters. 43 (6): 923. doi:10.1016/S0040-4039(01)02294-8.
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