Hexamethylphosphoramide → Allyl-hex-2-ynyl-carbamic acid tert-butyl ester

HRID 1182242Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1182242
[C:1]([O:5][C:6](=[O:14])[N:7]([CH2:11][CH:12]=[CH2:13])[CH2:8][C:9]#[CH:10])([CH3:4])([CH3:3])[CH3:2].[CH2:15]([Li])[CH2:16][CH2:17]C.CN(C)P(N(C)C)(N(C)C)=O.ICCC>O1CCCC1>[C:1]([O:5][C:6](=[O:14])[N:7]([CH2:11][CH:12]=[CH2:13])[CH2:8][C:9]#[C:10][CH2:15][CH2:16][CH3:17])([CH3:4])([CH3:3])[CH3:2]

Komponenten

6

Edukt 4

HCID 12679HexamethylphosphoramideHCID 336431-IodopropaneHCID 10863781tert-Butyl allyl(prop-2-yn-1-yl)carbamateHCID 178418339Butyllithium

Produkt 1

HCID 86600396Allyl-hex-2-ynyl-carbamic acid tert-butyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

A solution of allyl-prop-2-ynyl-carbamic acid tert-butyl ester (prepared in the manner described by Boger et al., J. Am. Chem. Soc., 1996, 118, 2109; 1.95 g) in anhydrous tetrahydrofuran (10 mL) was stirred at 0° C. in a cooling bath and treated with n-butyllithium (1.6 M solution in hexane; 7.2 mL) during a 5 min period. After being stirred for an additional 5 min, the solution was treated sequentially with hexamethylphosphoramide (2 mL) and a solution of 1-iodopropane (1.71 mL) in tetrahydrofuran (2 mL). After 65 min, the cooling bath was removed and the mixture was allowed to warm to room temperature where it stirred for 80 min. At the conclusion of this period, saturated aqueous ammonium chloride was added, followed by water to dissolve the solids. The mixture was extracted with ethyl acetate, and the combined organic phases were washed with saturated aqueous sodium chloride, dried over sodium sulfate and concentrated to yield a residue. The residue was purified by flash chromatography to provide a pale yellowish oil (1.67 g). MS (ES+) m/z 238.27 (M+H+).

Aufarbeitung

  1. waitAfter 65 min
  2. customthe cooling bath was removed
  3. stirringstirred for 80 min
  4. additionAt the conclusion of this period, saturated aqueous ammonium chloride was added
  5. dissolutionto dissolve the solids
  6. extractionThe mixture was extracted with ethyl acetate
  7. washthe combined organic phases were washed with saturated aqueous sodium chloride
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated
  10. customto yield a residue
  11. customThe residue was purified by flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-547f865a3d2d4c79aec52ffa52c1f206
Quelldatensatz
uspto-grants-2007_10
Patentnummer
US07288563B2

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