Reaktion #47307

Reaktionsgleichung

(S)-4-(2-allyloxy-pent-4-enyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid t-butyl ester

→

(S)-4-(3,6-dihydro-2H-pyran-2-ylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid t-butyl ester

Ausbeute 92.0%

Lösungsmittel

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeSolvents were evaporated
2. 2
   Sonstigethe residue was purified through flash column chromatography (silica gel, 0-20% ethyl acetate/hexanes)

Vorschrift

To a solution of (S)-4-(2-allyloxy-pent-4-enyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid t-butyl ester (1.38 g, 4.24 mmol) in dichloromethane (10 mL) was added benzylidene[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro-(tricyclohexylphosphine)ruthenium (144 mg, 4% equivalent). The mixture was stirred at room temperature for 4 h. Solvents were evaporated and the residue was purified through flash column chromatography (silica gel, 0-20% ethyl acetate/hexanes) to afford (S)-4-(3,6-dihydro-2H-pyran-2-ylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid t-butyl ester (1.16 g, 92%) as a brown oil: 1H NMR (300 MHz, CDCl3) δ ppm 1.48 (s, 12H), 1.56, 16.0 (2×s, 3H), 1.69 (br. s., 1H), 1.81-2.20 (m, 3H), 3.55 (br. s., 1H), 3.83-4.02 (m, 2H), 4.00-4.28 (m, 3H), 5.61-5.93 (m, 2H).

Quelle