TY - JOUR
T1 - Integrated micro flow synthesis based on sequential Br-Li exchange reactions of p-, m-, and o-dibromobenzenes
AU - Nagaki, Aiichiro
AU - Tomida, Yutaka
AU - Usutani, Hirotsugu
AU - Kim, Heejin
AU - Takabayashi, Naofumi
AU - Nokami, Toshiki
AU - Okamoto, Hideho
AU - Yoshida, Jun Ichi
PY - 2007
Y1 - 2007
N2 - A micro flow system consisting of micromixers and microtube reactors provides an effective method for the introduction of two electrophiles onto p-, m-, and o-dibromobenzenes. The Br-Li exchange reaction of p-dibromobenzene with nBuLi can be conducted by using the micro flow system at 20°C, although much lower temperatures (< -48°C) are needed for a batch reaction. The resulting p-bromophenyl-lithium was allowed to react with an electrophile in the micro flow system at 20°C. The p-substituted bromobenzene thus obtained was subjected to a second Br-Li exchange reaction followed by reaction with a second electrophile at 20°C in one flow. A similar transformation can be carried out with m-dibromobenzene by using the micro flow system. However, the Br-Li exchange reaction of o-dibromobenzene followed by reaction with an electrophile should be conducted at -78°C to avoid benzyne formation. The second Br-Li exchange reaction followed by reaction with an electrophile can be carried out at 0°C. By using the present method, a variety of p-, m-, and o-disubstituted benzenes were synthesized in one flow at much higher temperatures than are required for conventional batch reactions.
AB - A micro flow system consisting of micromixers and microtube reactors provides an effective method for the introduction of two electrophiles onto p-, m-, and o-dibromobenzenes. The Br-Li exchange reaction of p-dibromobenzene with nBuLi can be conducted by using the micro flow system at 20°C, although much lower temperatures (< -48°C) are needed for a batch reaction. The resulting p-bromophenyl-lithium was allowed to react with an electrophile in the micro flow system at 20°C. The p-substituted bromobenzene thus obtained was subjected to a second Br-Li exchange reaction followed by reaction with a second electrophile at 20°C in one flow. A similar transformation can be carried out with m-dibromobenzene by using the micro flow system. However, the Br-Li exchange reaction of o-dibromobenzene followed by reaction with an electrophile should be conducted at -78°C to avoid benzyne formation. The second Br-Li exchange reaction followed by reaction with an electrophile can be carried out at 0°C. By using the present method, a variety of p-, m-, and o-disubstituted benzenes were synthesized in one flow at much higher temperatures than are required for conventional batch reactions.
KW - Arenes
KW - Flow reactions
KW - Integrated micro flow synthesis
KW - Lithiation
KW - Microreactors
UR - http://www.scopus.com/inward/record.url?scp=36949023573&partnerID=8YFLogxK
U2 - 10.1002/asia.200700231
DO - 10.1002/asia.200700231
M3 - Article
C2 - 17935095
AN - SCOPUS:36949023573
SN - 1861-4728
VL - 2
SP - 1513
EP - 1523
JO - Chemistry - An Asian Journal
JF - Chemistry - An Asian Journal
IS - 12
ER -