2024-03-29T13:13:24Zhttp://digital.csic.es/dspace-oai/requestoai:digital.csic.es:10261/1638412020-04-28T11:19:26Zcom_10261_152009com_10261_8col_10261_160458
2018-04-19T10:33:56Z
urn:hdl:10261/163841
The reaction between triphenylphosphine and methyl 2-bromoalkanoates
Pórtulas, Joan
Sánchez, Francisco
Sánchez-Pardo, Josep
2 pages, 1 table
Because of the versatile applications of the Wittig reaction, the Touer (1-nethoxycarbonylalkvl)triphenylphosphonium bromides 1 (R * H, Ne) are uell characterized, useful synthetic intermediates. The higher members of the series, however, have I not been isolated, with the exception of ethyl esters 1 (R * Et or n-Bu, ethyl esters instead of methyl esters)1, 2. On the other hand, the obvious preparation of salts 1, namely the reaction between triphenylphosphine 2 and a methyl 2-bromoalkanoate 3, has not been the subject of a systematic study, although it can be concluded from literature data that vigorous reaction conditions and/or long reaction times are needed for the preparation of the higher members of the series 3. Finally, it is also known that several salts of type 1 (R - H, Ph, Ac) can decompose thermally 4.5, givlng methyl bromide, carbon dioxide, ylid 6 and salt 7 (Scheme)
2018-04-19T10:33:56Z
2018-04-19T10:33:56Z
1976-10
artículo
Tetrahedron Letters 17(40): 3617-3618 (1976)
0040-4039
http://hdl.handle.net/10261/163841
10.1016/S0040-4039(00)92975-7
eng
https://doi.org/10.1016/S0040-4039(00)92975-7
Sí
closedAccess
Elsevier