Reaktion #1561465

ord-939629442abf4ce18e2b0aecee610572

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction was quenched with water and aqueous sodium hydroxide (1 N, 2 mL)
  2. 2
    workup.STIRRINGThe contents were stirred for 3 h
  3. 3
    Extraktionextracted with EtOAc
  4. 4
    SonstigeThe organic layer was dried
  5. 5
    Einengenconcentrated

Vorschrift

A solution of 5-bromo-3,4-dihydro-1H-isochromene-1-carboxylic acid (0.500 g, 1.94 mmol) in 1 mL of THF was added BH3.THF (3.88 mL, 3.88 mmol) drop wise at 0° C. The mixture was stirred at 0° C. for 2 h. The reaction was quenched with water and aqueous sodium hydroxide (1 N, 2 mL). The contents were stirred for 3 h, and then extracted with EtOAc. The organic layer was dried and concentrated to give (5-bromo-3,4-dihydro-1H-isochromen-1-yl)methanol

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09018211B2uspto-grants-2015_04