External Trapping of Halomethyllithium Enabled by Flow Microreactors

被引:59
作者
Degennaro, Leonardo [1 ,2 ]
Fanelli, Flavio [1 ,2 ]
Giovine, Arianna [1 ,2 ]
Luisi, Renzo [1 ,2 ]
机构
[1] Univ Bari A Moro, Dept Pharm Drug Sci, FLAME Lab Flow Chem, I-70125 Bari, Italy
[2] Microreactor Technol Lab, I-70125 Bari, Italy
关键词
carbenoids; flow chemistry; microreactor technology; organolithiums; sustainable chemistry; FLASH CHEMISTRY; CHLOROMETHYL-LITHIUM; CARBONYL-COMPOUNDS; ADDITION-REACTIONS; AZIRIDINES; KETONES; DIIODOMETHYLLITHIUM; IODOMETHYLLITHIUM; TRANSFORMATION; CARBENOIDS;
D O I
10.1002/adsc.201400747
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This work demonstrates that the accurate control of the reaction parameters realized within microreactor systems allowed for a taming of the reactivity of thermally unstable intermediates such as haloalkyllithiums. The first example of effective external trapping of a reactive carbenoid such as the chloromethyllithium is described. By using microreactor systems, a continuous flow synthesis of chloro alcohols and chloro amines could be achieved with high yields. By controlling the residence time the highly reactive chloromethyllithium could be generated and reacted with electrophiles at temperatures much higher than in batch-mode and without internal quenching. The developed continuous-flow process matches the requirements for sustainability.
引用
收藏
页码:21 / 27
页数:7
相关论文
共 54 条
[1]   Preparation and synthetic applications of enantiopure (2S,3S)- or (2R,3S)-2-halomethyl-1,2-epoxyalkan-3-amines [J].
Barluenga, J ;
Baragaña, B ;
Concellón, JM .
JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (08) :2843-2846
[2]   PREPARATION OF DISUBSTITUTED EPICHLOROHYDRINS WITH TOTAL DIASTEREOSELECTIVITY - TRANSFORMATION OF ALPHA-BROMOCARBONYL COMPOUNDS INTO ALLYL ALCOHOLS [J].
BARLUENGA, J ;
LLAVONA, L ;
BERNAD, PL ;
CONCELLON, JM .
TETRAHEDRON LETTERS, 1993, 34 (19) :3173-3176
[3]   THE FIRST DIRECT PREPARATION OF CHIRAL FUNCTIONALIZED KETONES AND THEIR SYNTHETIC USES [J].
BARLUENGA, J ;
BARAGANA, B ;
ALONSO, A ;
CONCELLON, JM .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1994, (08) :969-970
[4]   HIGHLY DIASTEREOSELECTIVE SYNTHESIS OF THREO OR ERYTHRO AMINOALKYL EPOXIDES FROM ALPHA-AMINO-ACIDS [J].
BARLUENGA, J ;
BARAGANA, B ;
CONCELLON, JM .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (21) :6696-6699
[5]   Synthesis of enantiopure α′-amino α,β-epoxy ketones from α′-amino bromomethyl ketones [J].
Barluenga, J ;
Baragaña, B ;
Concellón, JM ;
Piñera-Nicolás, A ;
Díaz, MR ;
García-Granda, S .
JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (14) :5048-5052
[6]   FACILE ONE-POT TRANSFORMATION OF CARBOXYLIC-ACID CHLORIDES INTO 2-SUBSTITUTED ALLYL ALCOHOLS OR EPICHLOROHYDRINS [J].
BARLUENGA, J ;
FERNANDEZSIMON, JL ;
CONCELLON, JM ;
YUS, M .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1989, (01) :77-80
[7]   The electrophilic nature of carbenoids, nitrenoids, and oxenoids [J].
Boche, G ;
Lohrenz, JCW .
CHEMICAL REVIEWS, 2001, 101 (03) :697-756
[8]   Synthesis of cis-C-Iodo-N-Tosyl-Aziridines using Diiodomethyllithium: Reaction Optimization, Product Scope and Stability, and a Protocol for Selection of Stationary Phase for Chromatography [J].
Boultwood, Tom ;
Affron, Dominic P. ;
Trowbridge, Aaron D. ;
Bull, James A. .
JOURNAL OF ORGANIC CHEMISTRY, 2013, 78 (13) :6632-6647
[9]   The Synthesis of Bromomethyltrifluoroborates through Continuous Flow Chemistry [J].
Broom, Toby ;
Hughes, Mark ;
Szczepankiewicz, Bruce G. ;
Ace, Karl ;
Hagger, Ben ;
Lacking, Gary ;
Chima, Ranjit ;
Marchbank, Graeme ;
Alford, Gareth ;
Evans, Paul ;
Cunningham, Christopher ;
Roberts, John C. ;
Perni, Robert B. ;
Berry, Malcolm ;
Rutter, Andrew ;
Watson, Simon A. .
ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2014, 18 (11) :1354-1359
[10]   Highly cis-selective synthesis of iodo-aziridines using diiodomethyllithium and in situ generated N-Boc-imines [J].
Bull, James A. ;
Boultwood, Tom ;
Taylor, Thomas A. .
CHEMICAL COMMUNICATIONS, 2012, 48 (100) :12246-12248