Abstract
New routes to alkoxymaleic anhydrides 1a /b have been described in good yields via
base-induced chemoselective vinylic substitution of bromo atom in
bromomaleimide 4 with alkanols, and base-induced
oxa-Micahel addition of alkanols to dialkyl acetylenedicarboxylates 8a /b as
key steps. An unusual acyl exchange in the conversion of 6a /b to 1a /b under
very simple and mild reaction conditions is noteworthy.
Key words
bromomaleimide - dialkyl acetylenedicarboxylates - oxa-Michael additions - alkoxymaleic
anhydrides
References <A NAME="RZ13302SS-1">1 </A>
NCL Communication No. 6633.
<A NAME="RZ13302SS-2A">2a </A>
Pattenden G.
Fortsch. Chem. Org. Naturstoffe
1978,
35:
133
<A NAME="RZ13302SS-2B">2b </A>
Gaudreault RC, and
Mongrain C. inventors; PCT
Int. Appl. WO 9108775.
; Chem. Abstr. 1991 , 115 , 183069
<A NAME="RZ13302SS-2C">2c </A>
Becker R, and
Rohr W. inventors; Eur. Pat. Appl. Ep 289925.
; Chem. Abstr. 1989 , 111 , 40070
<A NAME="RZ13302SS-3">3 </A>
Stachel H.-D.
Schachtner J.
Seidel J.
Z.
Naturforsch., B: Chem. Sci.
1996,
51:
409
<A NAME="RZ13302SS-4">4 </A>
Yeh C.-L.
Colwell WT.
DeGraw JI.
Tetrahedron Lett.
1978,
42:
3987
<A NAME="RZ13302SS-5">5 </A>
Stachel H.-D.
Schachtner J.
Z. Naturforsch., B: Chem.
Sci.
1996,
51:
1334
<A NAME="RZ13302SS-6">6 </A>
Clemo NG.
Gedge DR.
Pattenden G.
J.
Chem. Soc., Perkin Trans. 1
1981,
1448
<A NAME="RZ13302SS-7A">7a </A>
Kayser MM.
Hatt KL.
Yu H.
Hopper DL.
Can. J.
Chem.
1993,
71:
1010
<A NAME="RZ13302SS-7B">7b </A>
Kayser MM.
Breau L.
Tetrahedron
Lett.
1988,
29:
6203
<A NAME="RZ13302SS-8A">8a </A>
Wel HVD.
Nibbering NMM.
Can. J. Chem.
1988,
66:
2587
<A NAME="RZ13302SS-8B">8b </A>
Kayser MM.
Breau L.
Eliev S.
Morland P.
Ip HS.
Can.
J. Chem.
1986,
64:
104
<A NAME="RZ13302SS-8C">8c </A>
Kayser MM.
Eisenstein O.
Can.
J. Chem.
1981,
59:
2457
<A NAME="RZ13302SS-9">9 </A>
Balasubramaniyan V.
Balasubramaniyan P.
Shaikh AS.
Argade NP.
Indian
J. Chem., Sect. B
1989,
28:
123
<A NAME="RZ13302SS-10A">10a </A>
James GD.
Pattenden G.
Mills SD.
Tetrahedron Lett.
1985,
26:
3617
<A NAME="RZ13302SS-10B">10b </A>
Gill GB.
James GD.
Oates KV.
Pattenden G.
J.
Chem. Soc., Perkin Trans. 1
1993,
2567
<A NAME="RZ13302SS-10C">10c </A>
James GD.
Mills SD.
Pattenden G.
J. Chem. Soc., Perkin Trans. 1
1993,
2581
<A NAME="RZ13302SS-11">11 </A>
Ralph RK.
Shaw G.
Naylor RN.
J.
Chem. Soc.
1959,
1169
<A NAME="RZ13302SS-12A">12a </A>
Roberts JC.
J. Chem. Soc.
1952,
3315
<A NAME="RZ13302SS-12B">12b </A>
Owen TC.
Austin DJ.
J.
Org. Chem.
1993,
58:
756
<A NAME="RZ13302SS-13A">13a </A>
Adlington RM.
Baldwin JE.
Cox RJ.
Pritchard GJ.
Synlett
2002,
820
<A NAME="RZ13302SS-13B">13b </A>
Li J.
Li G.
Jiang H.
Chen M.
Tetrahedron Lett.
2001,
42:
6923 ; and references 13a,b cited therein
<A NAME="RZ13302SS-14">14 </A>
Mhaske, S. B.; Argade, N. P., unpublished
results.
<A NAME="RZ13302SS-15A">15a </A>
Kar A.
Argade NP.
Tetrahedron
Lett.
2002,
43:
6563
<A NAME="RZ13302SS-15B">15b </A>
Kar A.
Argade NP.
J. Org. Chem.
2002,
67:
7131
<A NAME="RZ13302SS-15C">15c </A>
Mangaleswaran S.
Argade NP.
Synthesis
2002,
865 ; and references 15a-c cited therein
<A NAME="RZ13302SS-16">16 </A>
Kar A.
Argade NP.
Synthesis
2002,
221
<A NAME="RZ13302SS-17A">17a </A>
Mangaleswaran S.
Argade NP.
J.
Chem. Soc., Perkin Trans. 1
2000,
3290
<A NAME="RZ13302SS-17B">17b </A>
Mangaleswaran S.
Argade NP.
J.
Chem. Soc., Perkin Trans. 1
2001,
1764
<A NAME="RZ13302SS-18">18 </A>
Ratemi ES.
Dolence JM.
Poulter CD.
Vederas JC.
J.
Org. Chem.
1996,
61:
6296
<A NAME="RZ13302SS-19">19 </A>
The
Merck Index
Merck & Co., Inc.;
Rahway:
1996.
12th ed..
p.1218
<A NAME="RZ13302SS-20">20 </A>
Reddy PY.
Kondo S.
Toru T.
Ueno Y.
J. Org. Chem.
1997,
62:
2652