Reaktion #57070

ord-88e7ded5a61e46328892f889f67ed6cb

Reaktionsgleichung

CCN(CC)CC.Cl
triethylamine hydrochloride
C1CCOC1
THF
CC(=O)[O-].[Na+]
sodium acetate
CC(=O)O[C@@H]1C=Cc2ccccc2[C@H]1O
2
CC(=O)O[C@@H]1C=Cc2ccccc2[C@H]1O
(1R*,2R*)-Acetic acid 1-hydroxy-1,2-dihydro-naphthalen-2-yl-ester

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeTo a flame dried round bottom flask
  2. 2
    TemperaturThe mixture was heated
  3. 3
    Temperaturat reflux for 3 hours
  4. 4
    Sonstigethe solvents were removed in vacuio
  5. 5
    SonstigeThe resulting mixture was purified by flash chromatography (30% ethyl acetate in hexanes)

Vorschrift

To a flame dried round bottom flask, [Rh(COD)Cl]2 (4.3 mg, 0.008 mmol DPPF (9.6 mg, 0.017 mmol),1 (50 mg, 1.39 mmol), and sodium acetate (142 mg, 1.74 mmol) were added followed by addition of THF (2 mL) and triethylamine hydrochloride (239 mg, 1.74 mmol). The mixture was heated at reflux for 3 hours and the solvents were removed in vacuio. The resulting mixture was purified by flash chromatography (30% ethyl acetate in hexanes) to give 2 as a crystalline solid (41 mg), 63%). Rf=0.26 on silica gel (20% ethyl acetate:hexanes); mp 67-68° (Et2O); IR (KBr, cm−1) 1H NMR (400 MHz, CDCl3) δ 7.54-7.53 (1H, m), 7.29-7.24 (2H, m), 7.10-7.08 (1H, m), 6.50 (1H, dd, J=3.9, 1.3 Hz), 5.85 (1H, dd, J=9.9, 3.1 Hz), 5.59 (1H, ddd, J=9.0, 2.8, 1.9 Hz), 4.92 (1H, d, J=9.0 Hz), 2.64 (1H, s), 2.12 (3H, s); 13C NMR (400 MHz, CDCl3) δ 171.3, 135.2, 131.5, 129.5, 128.3, 126.7, 126.0, 125.4, 75.3, 71.7, 21.2. HRMS calcd for C12H12O3 (M+): 204.0786. Found: 204.0791.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07420003B2uspto-grants-2008_09