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Technology Process of C48H53BF2N6

C48H53BF2N6

Base Information
  • Chemical Name:C48H53BF2N6
  • CAS No.:1431609-43-6
  • Molecular Formula:C48H53BF2N6
  • Molecular Weight:762.797
  • Hs Code.:
C<sub>48</sub>H<sub>53</sub>BF<sub>2</sub>N<sub>6</sub>

Synonyms:

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Chemical Property of C48H53BF2N6
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Technology Process of C48H53BF2N6

There total 1 articles about C48H53BF2N6 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 34.0%

formyl meso-octamethylcalix[4]pyrrole
312303-98-3

formyl meso-octamethylcalix[4]pyrrole

phenyl BODIPY

phenyl BODIPY

C<sub>77</sub>H<sub>87</sub>BF<sub>2</sub>N<sub>10</sub>
1431609-42-5

C77H87BF2N10

C<sub>48</sub>H<sub>53</sub>BF<sub>2</sub>N<sub>6</sub>
1431609-43-6

C48H53BF2N6

Guidance literature:
With piperidine; toluene-4-sulfonic acid; In toluene; for 2h; Inert atmosphere; Dean-Stark; Molecular sieve; Reflux;
DOI:10.1002/ejoc.201201504

Reference yield: 27.0%

C<sub>48</sub>H<sub>53</sub>BF<sub>2</sub>N<sub>6</sub>
1431609-43-6

C48H53BF2N6

4-(1,4,7,10,13-pentaoca-16-azacyclohexadecan-16-yl)benzaldehyde
73171-36-5

4-(1,4,7,10,13-pentaoca-16-azacyclohexadecan-16-yl)benzaldehyde

C<sub>67</sub>H<sub>80</sub>BF<sub>2</sub>N<sub>7</sub>O<sub>5</sub>

C67H80BF2N7O5

Guidance literature:
With piperidine; In toluene; for 2h; Dean-Stark; Molecular sieve; Inert atmosphere; Reflux;
DOI:10.1002/ejoc.201402214

Reference yield:

C<sub>48</sub>H<sub>53</sub>BF<sub>2</sub>N<sub>6</sub>
1431609-43-6

C48H53BF2N6

C<sub>67</sub>H<sub>80</sub>BF<sub>2</sub>N<sub>7</sub>O<sub>5</sub>*C<sub>4</sub>H<sub>9</sub>NO<sub>2</sub>

C67H80BF2N7O5*C4H9NO2

Guidance literature:
Multi-step reaction with 2 steps
1: piperidine / toluene / 2 h / Dean-Stark; Molecular sieve; Inert atmosphere; Reflux
2: acetonitrile / 24 h / Darkness
With piperidine; In toluene; acetonitrile; 1: |Knoevenagel Condensation;
DOI:10.1002/ejoc.201402214
upstream raw materials:

formyl meso-octamethylcalix[4]pyrrole

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