Imidazole → ((s)-3-Iodo-1-methoxymethyl-propyl)-carbamic acid tert-butyl ester

HRID 1182122Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1182122
[I:1]I.N1C=CN=C1.[C:8]([O:12][C:13](=[O:22])[NH:14][C@H:15]([CH2:19][O:20][CH3:21])[CH2:16][CH2:17]O)([CH3:11])([CH3:10])[CH3:9]>ClCCl>[C:8]([O:12][C:13](=[O:22])[NH:14][C@H:15]([CH2:19][O:20][CH3:21])[CH2:16][CH2:17][I:1])([CH3:11])([CH3:10])[CH3:9]

Komponenten

5

Versuchsvorschrift

A suspension of polystyrene resin-bound triphenylphosphine (18.645 g, 3 mmol/g) in dry dichloromethane (250 ml) is treated with iodine (12.5 g, 49.22 mmol) and stirred for 15 minutes under argon. Imidazole (3.87 g, 55.94 mmol) is added and the reaction mixture stirred at room temperature for a further 15 minutes. The reaction mixture is then treated with a solution of ((S)-3-Hydroxy-1-methoxymethyl-propyl)-carbamic acid tert-butyl ester (4.9 g, 22.37 mmol) in dichloromethane (30 ml), and refluxed for 1.5 hours under argon. The resin is removed by filtration through a celite pad, washing with dichloromethane. The filtrate is washed with 5% aqueous sodium thiosulphate solution and water, dried over MgSO4 and evaporated to afford ((S)-3-Iodo-1-methoxymethyl-propyl)-carbamic acid tert-butyl ester as a crude oil. [M-BOC] 230.06.

Aufarbeitung

  1. stirringthe reaction mixture stirred at room temperature for a further 15 minutes
  2. temperaturerefluxed for 1.5 hours under argon
  3. customThe resin is removed by filtration through a celite pad
  4. washwashing with dichloromethane
  5. washThe filtrate is washed with 5% aqueous sodium thiosulphate solution and water
  6. dry with materialdried over MgSO4
  7. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-75e5c7ae8e85446c9f4e6571ebc35a00
Quelldatensatz
uspto-grants-2007_10
Patentnummer
US07288537B2

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