Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 1513-1523 |
| Number of pages | 11 |
| Journal | Chemistry - An Asian Journal |
| Volume | 2 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 2007 |
| Externally published | Yes |
Keywords
- Arenes
- Flow reactions
- Integrated micro flow synthesis
- Lithiation
- Microreactors
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry