Reaktion #8858

ord-9ec86a96bfa746418eba080ec0d772d5

Reaktionsgleichung

CC(C)(C)[Si](C)(C)Cl
tert-butyldimethylsilyl chloride
C=CC1C(O)CCC12CCN(C(=O)OC(C)(C)C)CC2
tert-butyl 1-vinyl-2-hydroxy-8-azaspiro[4.5]decane-8-carboxylate
c1c[nH]cn1
imidazole
C=CC1C(O[Si](C)(C)C(C)(C)C)CCC12CCN(C(=O)OC(C)(C)C)CC2
title compound
Ausbeute 86.2%
C=CC1C(O[Si](C)(C)C(C)(C)C)CCC12CCN(C(=O)OC(C)(C)C)CC2
tert-Butyl 1-vinyl-2-(tert-butyldimethylsilyloxy)-8-azaspiro[4.5]decane-8-carboxylate
Ausbeute 86.2%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe mixture was extracted twice with ether
  2. 2
    WaschenThe combined ether layers were washed with brine
  3. 3
    Trocknendried over sodium sulfate
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated
  6. 6
    SonstigeThe residue was purified by flash chromatography
  7. 7
    Wascheneluting with 5% ethyl acetate in hexanes

Vorschrift

To a solution of tert-butyl 1-vinyl-2-hydroxy-8-azaspiro[4.5]decane-8-carboxylate (0.462 g, 1.64 mmoL) from Step A in DMF (8 mL) was added imidazole (0.335 mg, 4.92 mmol) and then tert-butyldimethylsilyl chloride (0.370 g, 2.4 mmol). The reaction was stirred at room temperature for 20 h and then diluted with ether and sodium bicarbonate solution. The mixture was extracted twice with ether. The combined ether layers were washed with brine, dried over sodium sulfate, filtered, and concentrated. The residue was purified by flash chromatography eluting with 5% ethyl acetate in hexanes to afford the title compound (0.56 g) as a mixture of isomers.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091211B2uspto-grants-2006_08