Reaktion #49853

ord-41bf4b14ae7e4194a8b652aa27b29dc4

Reaktionsgleichung

O=c1cc(-c2ccsc2)c2ccc(CO)cc2o1
alcohol
O=c1cc(-c2ccsc2)c2ccc(CO)cc2o1
7-Hydroxymethyl-4-(3-thienyl)coumarin
CN(C)P(N(C)C)N(C)C
hexamethylphosphorous triamide
ClC(Cl)(Cl)Cl
CCl4
O=c1cc(-c2ccsc2)c2ccc(CCl)cc2o1
title compound
O=c1cc(-c2ccsc2)c2ccc(CCl)cc2o1
7--Chloromethyl-4-(3-thienyl)coumarin

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationfiltered
  2. 2
    Einengenconcentrated
  3. 3
    Sonstigethe residue chromatographed (30% EtOAc/hexane)

Vorschrift

To a solution of the alcohol from Step 1 (1.65 g) and hexamethylphosphorous triamide in 35 mL THF at 0° C. was added CCl4 (1.3 mL) and the mixture stirred for 30 min. The mixture was diluted with Et2O, filtered, concentrated and the residue chromatographed (30% EtOAc/hexane) to provide the title compound as a solid, m.p. 125°-127° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05424320uspto-grants-1995_06