Réaction #2358557

ord-c643e8329fe243edb9457c62154a01e6

Équation de réaction

O=C1c2ccc(S(=O)(=O)Cl)cc2C(=O)c2cc(S(=O)(=O)Cl)ccc21
Anthraquinone-2,7-disulfonylchloride
CCN(C(C)C)C(C)C
diisopropylethylamine
O=C1c2ccc(S(=O)(=O)N3CCCCCCC3)cc2C(=O)c2cc(S(=O)(=O)N3CCCCCCC3)ccc21
yellow compound 1-27
Rendement 91.0%
O=C1c2ccc(S(=O)(=O)N3CCCCCCC3)cc2C(=O)c2cc(S(=O)(=O)N3CCCCCCC3)ccc21
2,7-bis(azocan-1-ylsulfonyl)anthracene-9,10-dione
Rendement 91.0%

Solvants

Conditions de réaction

Température
-50°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreSolvent was evaporated
  2. 2
    workup.ADDITIONthe residue was treated with 1N HCl
  3. 3
    Filtrationfiltered off
  4. 4
    Lavagewashed with water
  5. 5
    Autredried
  6. 6
    AutreCrude material was crystallized from chloroform-hexane

Mode opératoire

Anthraquinone-2,7-disulfonylchloride (1215 mg, 3 mmole) was dissolved in 100 mL DCM. The solution was cooled to −50° C. To this solution was added 1 mL (8 mmole) of heptamethyleneimine, followed by 1 mL of diisopropylethylamine. The reaction mixture was stirred at room temperature for 4 hrs. Solvent was evaporated and the residue was treated with 1N HCl, filtered off, washed with water and dried. Crude material was crystallized from chloroform-hexane to give 1.014 g (91%) of yellow compound 1-27. H1—NMR (CDCl3): 8.70 (2H, d, C1 and C8), 8.47 (2H, d, C4 and C5), 8.22 (2H, dd, C3 and C6), 3.22 (8H, m), 1.70 (20H, m).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09120754B2uspto-grants-2015_09