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Trifluoroacetic acid → (3R)-3-[(Benzylthio)methyl]pyrrolidine

HRID 1459716
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1459716
[CH2:1]([S:8][CH2:9][C@@H:10]1[CH2:14][CH2:13][N:12](C(OC(C)(C)C)=O)[CH2:11]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.FC(F)(F)C(O)=O>ClCCl>[CH2:1]([S:8][CH2:9][C@@H:10]1[CH2:14][CH2:13][NH:12][CH2:11]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 6422Trifluoroacetic acidHCID 54246072(3R)-3-(Benzylthio)methyl-1-(tert-butoxycarbonyl)pyrrolidine

Produkt 1

HCID 53700038(3R)-3-[(Benzylthio)methyl]pyrrolidineAusbeute 77,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a stirred solution of (3R)-3-(benzylthio)methyl-1-(tert-butoxycarbonyl)pyrrolidine (0.2320 g, 0.755 mmol) in dichloromethane (3 ml), under argon, was added trifluoroacetic acid (1 ml) and the mixture was stirred at room temperature for 65 minutes before quenching with anhydrous methanol (2 ml) and evaporating in vacuo. More methanol (2 ml) was added to the residue and removed in vacuo. The residual oil was then dissolved in dichloromethane (25 ml) and washed with 2N NaOH solution (10 ml). The aqueous layer was reextracted with more dichloromethane (15 ml) and the combined dichloromethane extracts were washed with saturated NaCl solution (10 ml), dried (Na2SO4) and evaporated in vacuo. The residue was purified by flash chromatography (silica gel, CH2Cl2 /MeOH/NH3, 85:15:1.5) to give 0.1210 g (77%) of the title compound as a colourless oil. δH (250 MHz,CDCl3) 1.41 (1H, m), 1.90-2.00 (1H, m), 2.24 (1H, m), 2.42-2.50 (2H, m), 2.57 (1H, dd, J=6.5 and 11.0 Hz), 2.82-2.99 (2H, m), 3.07 (1H, dd, J=7.3 and 11.0 Hz), 3.72 (2H, s), 7.20-7.36 (5H, m); m/e (ES) 208 (M+ +1).

Aufarbeitung

  1. custombefore quenching with anhydrous methanol (2 ml)
  2. customevaporating in vacuo
  3. additionMore methanol (2 ml) was added to the residue
  4. customremoved in vacuo
  5. dissolutionThe residual oil was then dissolved in dichloromethane (25 ml)
  6. washwashed with 2N NaOH solution (10 ml)
  7. washthe combined dichloromethane extracts were washed with saturated NaCl solution (10 ml)
  8. dry with materialdried (Na2SO4)
  9. customevaporated in vacuo
  10. customThe residue was purified by flash chromatography (silica gel, CH2Cl2 /MeOH/NH3, 85:15:1.5)

Quellen und Nachweise

ORD-Eintrag
ord-c8b0c20581a84c578cbc8ce010139b23
Quelldatensatz
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05854268

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