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Imidazole → tert-butyl (3R)-3-(iodomethyl)pyrrolidine-1-carboxylate

HRID 927983
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 927983
[I:1]I.N1C=CN=C1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O[CH2:28][C@@H:29]1[CH2:33][CH2:32][N:31]([C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])[CH2:30]1>C(OCC)C.O1CCOCC1>[I:1][CH2:28][C@@H:29]1[CH2:33][CH2:32][N:31]([C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])[CH2:30]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 795ImidazoleHCID 807IodineHCID 11776TriphenylphosphineHCID 1514340tert-Butyl (3R)-3-(hydroxymethyl)pyrrolidine-1-carboxylate

Produkt 1

HCID 59371368tert-butyl (3R)-3-(iodomethyl)pyrrolidine-1-carboxylateAusbeute 93,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283
Diethyl Ether
Lösungsmittel
2×
HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

Iodine (1.91 g) was added in portions to a vigorously stirred, ice cooled suspension of imidazole (0.681 g) and triphenylphosphine (1.97 g) in diethyl ether (12 mL). The mixture was then stirred for 10 minutes before a solution of tert butyl (R)-3-hydroxymethylpyrrolidine-1-carboxylate (1 g) in dioxane (6 mL) was added dropwise. The resulting mixture was stirred at room temperature overnight, then diluted with diethyl ether and filtered. The solid was washed with diethyl ether and the combined filtrate was evaporated to dryness. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and pentane with a gradient of 0-20% to give tert-butyl (R)-3-iodomethylpyrrolidine-1-carboxylate (1.44 g) as an oil.

Aufarbeitung

  1. temperatureice cooled
  2. additionwas added dropwise
  3. stirringThe resulting mixture was stirred at room temperature overnight
  4. filtrationfiltered
  5. washThe solid was washed with diethyl ether
  6. customthe combined filtrate was evaporated to dryness
  7. customThe residue was purified by chromatography on silica
  8. washeluting with a mixture of ethyl acetate and pentane with a gradient of 0-20%

Quellen und Nachweise

ORD-Eintrag
ord-a1aee225980442869f46cc6d9fe4f392
Quelldatensatz
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09290472B2

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