Reaktion #40288

ord-c1a6f8c1a01b4e9980cd4e74051819a9

Reaktionsgleichung

O=c1c2ccccc2nnn1O
3-hydroxy-1,2,3-benzotriazin-4(3H)-one
CCC#CC(=O)O
Pentynoic acid
C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
O=c1c2ccccc2nnn1O
3-Hydroxy-1,2,3-benzotriazin-4(3H)-one
C#CCCC(=O)On1nnc2ccccc2c1=O
Pent-4-ynoic Acid 4-oxo-4H-benzo[d][1,2,3]triazin-3-yl Ester

Lösungsmittel

Reaktionsbedingungen

Temperatur
-10°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe solution was cooled in a brine-icewater bath
  2. 2
    Sonstige2 h
  3. 3
    Sonstigeat room temperature
  4. 4
    FiltrationPrecipitated salts were filtered off
  5. 5
    EinengenThe filtrate was concentrated in vacuo
  6. 6
    Sonstigecrystallized from hexane (4 mL)
  7. 7
    FiltrationThe crystals were filtered off
  8. 8
    Sonstigedried

Vorschrift

Pentynoic acid (200 mg, 2.04 mmol) was dissolved in THF (4 mL). The solution was cooled in a brine-icewater bath. A solution of dicyclohexylcarbodiimide (421 mg, 2.04 mmol) in THF (2 mL) was added. 3-Hydroxy-1,2,3-benzotriazin-4(3H)-one (333 mg, 2.04 mmol) was added after 5 minutes. The reaction mixture was stirred 1 h at −10° C. and then 2 h at room temperature. TLC indicated full conversion of 3-hydroxy-1,2,3-benzotriazin-4(3H)-one (eluent: ethyl acetate). Precipitated salts were filtered off. The filtrate was concentrated in vacuo and crystallized from hexane (4 mL). The crystals were filtered off and dried. Yield: 450 mg, 93%. RF=0.8 (ethyl acetate).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07727713B2uspto-grants-2010_06