Reaktion #43463

ord-479eea0990784411930dc1e50887c603

Reaktionsgleichung

CCOC1(OCC)CC2C(=O)CCC21
compound 1F
CCOC1(OCC)CC2C(=O)CCC21
6,6-Diethoxybicyclo[3.2.0]heptan-2-one
[BH4-].[Na+]
NaBH4
O=C1CC2C(O)CCC12
title compound
O=C1CC2C(O)CCC12
2-Hydroxybicyclo[3.2.0]heptan-6-one

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe reaction was concentrated
  2. 2
    workup.DISSOLUTIONdissolved in EtOAc
  3. 3
    Waschenwashed with water
  4. 4
    Trocknendried over Na2SO4
  5. 5
    Einengenconcentrated
  6. 6
    SonstigePurification by silica gel chromatography (50% EtOAc in hexanes)

Vorschrift

To a stirred solution of compound 1F in dioxane (50 mL) and 2M KH2PO4 (50 mL) was added NaBH4 (1.0 g, 26.4 mmol) over a 10 min-period, and the stirring was continued at RT for 1 hr. The reaction mixture was diluted with 2M HCl to adjust pH to 1, and stirred at RT for another 1 hr. The reaction was concentrated, dissolved in EtOAc, washed with water, dried over Na2SO4, and concentrated. Purification by silica gel chromatography (50% EtOAc in hexanes) provided the title compound (1.9 g) as a pale yellow oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732480B2uspto-grants-2010_06