Synthesis 2009(22): 3807-3818  
DOI: 10.1055/s-0029-1218117
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York

O,S-Dimethyl Carbonodithioate as a Phosgene Substitute for the Preparation of S-Methyl Alkylcarbamothioates and Dialkylcarbamothioates

Iacopo Degani, Rita Fochi*, Claudio Magistris
Dipartimento di Chimica Generale e Chimica Organica, Università degli Studi di Torino, C.so M. D’Azeglio 48, 10125 Torino, Italy
e-Mail: rita.fochi@unito.it;
Further Information

Publication History

Received 18 June 2009
Publication Date:
23 September 2009 (online)

Abstract

O,S-Dimethyl carbonodithioate is proposed as a suitable and safely handled reagent that can be used as a replacement for phosgene in the synthesis of S-methyl alkyl- and dialkylcarbamo-thioates. The former were obtained by a two-step procedure, which can also be carried out in a one-pot fashion without isolating the intermediates O-methyl alkylcarbamothioates; the overall yields of the pure S-methyl alkylcarbamothioates were 94-98%. Optimal conditions for the synthesis of S-methyl dialkylcarbamothioates involved a one-step procedure in a solvent-free system in the presence of triethyl(methyl)ammonium methyl carbonate as a catalyst; yields of the pure products were 85-98%. A mechanism is proposed for the carbamothioate-formation reaction.

    References

  • 2 Degani I. Fochi R. Regondi V. Synthesis  1981,  149 
  • 3a Degani I, Fochi R, and Regondi V. inventors; (CNR Italy) Patent EP  63327.  ; Chem. Abstr. 1983, 98, 160238
  • 3b Degani I. Fochi R. Regondi V. Synthesis  1983,  630 
  • 3c Degani I. Fochi R. Regondi V. Synthesis  1986,  1070 
  • 3d Cadamuro S. Degani I. Fochi R. Regondi V. Chem. Ind. (London)  1986,  671 
  • 3e Degani I, Fochi R, and Regondi V. inventors; (CNR, Italy) Patent IT  1173436. 
  • 4a Barbero M, Degani I, Fochi R, and Regondi V. inventors; (CNR, Italy) Patent EP  234249.  ; Chem. Abstr. 1988, 108, 23697
  • 4b Barbero M. Cadamuro S. Degani I. Fochi R. Regondi V. Synthesis  1989,  957 
  • For more information on the toxicity of phosgene, see for example:
  • 5a Lewis RJ. Sax’s Dangerous Properties of Industrial Materials   11th ed., Vol. 3:  Wiley; Hoboken: 2004.  p.2944-2945  
  • 5b Senet J.-P. In Recent Advances in Phosgene Chemistry   Vol. 1:  Société Nationale des Poudres et des Explosifs; Nanterre: 1997.  p.10-11  
  • 5c Cotarca L. Eckert H. Phosgenations: A Handbook   Wiley-VCH; Weinheim: 2003.  p.9 
  • 6 Artuso E. Carvoli G. Degani I. Fochi R. Magistris C. Synthesis  2007,  1096 
  • 7a Carvoli G, Degani I, Pallucca E, Fochi R, Gazzetto S, Artuso E, Lazzaroni M, and Cadamuro S. inventors; (Oxon Italia SpA) Patent IT  MI20051284. 
  • 7b Artuso E. Degani I. Fochi R. Magistris C. Synthesis  2008,  1612 
  • 7c Degani I. Fochi R. Magistris C. Synthesis  2008,  2919 
  • 8a Carvoli G, Degani I, Pallucca E, Fochi R, Serri AM, Cadamuro S, Gazzetto S, and Migliaccio M. inventors; (Oxon Italia SpA) Patent IT  MI2004002402. 
  • 8b Artuso E. Degani I. Fochi R. Magistris C. Synthesis  2007,  3497 
  • 8c Degani I. Fochi R. Magistris C. Migliaccio M. Synthesis  2009,  801 
  • 10 Pallucca E, Degani I, Serri AM, Fochi R, Gazzetto S, Fenoglio C, Ornati C, Migliaccio M, Cadamuro S, Carvoli G, and . inventors; Patent EP  1334965. A part of this study has been patented, see: ; Chem. Abstr. 2003, 139, 164529
  • For some examples of isomerizations of O-alkyl carbamothioates to the corresponding S-alkyl carbamo-thioates, see:
  • 11a Fujii K. Shuto Y. Kinoshita Y. Agric. Biol. Chem.  1990,  54:  2379 
  • 11b Tandel SK. Rajappa S. Pansare SV. Tetrahedron  1993,  49:  7479 
  • 11c Sakamoto M. Yoshiaki M. Takahashi M. Fujita T. Watanabe S. J. Chem. Soc., Perkin Trans. 1  1995,  373 
  • 11d Tandel SK, Naik RH, and Rajappa S. inventors; IN  175790.  (Council of Scientific and Industrial Research, India) ; Chem. Abstr. 2003, 139, 395632
  • 11e Harayama H. Nagahama T. Kozera T. Kimura M. Fugami K. Tanaka S. Tamaru Y. Bull. Chem. Soc. Jpn.  1997,  70:  445 
  • 11f Böhme A. Gais H.-J. Tetrahedron: Asymmetry  1999,  10:  2511 
  • 11g Gais H.-J. Böhme A. J. Org. Chem.  2002,  67:  1153 
  • 11h Milosavljevi MM. Marinkovi AD. Djordjevi SA. Hem. Ind.  2006,  60:  27 ; Chem. Abstr. 2006, 146, 461825
  • 11i Crich D. Brebion F. Krishnamurthy V. Org. Lett.  2006,  8:  3593 
  • 11j Crich D. Krishnamurthy V. Brebion F. Karatholuvhu M. Subramanian V. Hutton TK. J. Am. Chem. Soc.  2007,  129:  10282 
  • 11k Crich D, Brebion F, and Krishnamurthy V. inventors; (Olson & Hierl) Patent US  2007260041.  ; Chem. Abstr. 2007, 147, 522585
  • 14 Breme K. Fernandez X. Meierhenrich UJ. Brevard H. Joulain D. J. Agric. Food Chem.  2007,  55:  1932 
  • 15 Moffett RB. J. Chem. Eng. Data  1980,  25:  176 
  • 16 Burrows AA. Hunter L. J. Chem. Soc.  1952,  4118 
  • 17 Pontes RM. Basso EA. dos Santos FP. J. Org. Chem.  2007,  72:  1901 
  • 18 Lemire AE. Thompson JC. Can. J. Chem.  1970,  48:  824 
  • 19 Billeter JO. Ber. Dtsch. Chem. Ges.  1910,  43:  1853 
  • 20 Sonoda N. Mizuno T. Murakami S. Kondo K. Ogawa A. Ryu I. Kambe N. Angew. Chem., Int. Ed. Engl.  1989,  28:  452 ; Angew. Chem. 1989, 101, 476
  • 21 Mizuno T. Kino T. Ito T. Miyata T. Synth. Commun.  2000,  30:  1675 
  • 22 Hinterberger S. Hofer O. Greger H. Tetrahedron  1998,  54:  487 
  • 23 Leung M.-k. Lai J.-L. Lau K.-H. Yu H.-h. Hsiao H.-J. J. Org. Chem.  1996,  61:  4175 
  • 24 Tilles H. J. Am. Chem. Soc.  1959,  81:  714 
  • 25 Mizuno T. Mihara M. Nakai T. Iwai T. Ito T. Synthesis  2007,  3135 
1

Professor Emeritus, University of Turin, Italy.

9

For syntheses and applications of S-alkyl carbamothioates, particularly S-methyl carbamothioates, see Ref. 6 and references cited therein.

12

Degani, I.; Fochi, R.; Magistris, C. unpublished results.

13

Oxon Italia SpA., 20016 Pero (Milano), Italy.