Methanol → (2R,4R)-methyl 4-hydroxypyrrolidine-2-carboxylate

HRID 1796298

Reaktionsgleichung

Reaktionsgleichung von HRID 1796298
[OH:1][C@H:2]1[CH2:6][NH:5][C@@H:4]([C:7]([OH:9])=[O:8])[CH2:3]1.[CH3:10]O>>[CH3:10][O:8][C:7]([C@H:4]1[CH2:3][C@@H:2]([OH:1])[CH2:6][NH:5]1)=[O:9]

Komponenten

3

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Cis-4-Hydroxy-D-proline (15 g, 115 mmol) was suspended in 150 mL anhydrous methanol under an argon atmosphere, then cooled to 0° C. before bubbling in HCl gas for 15 minutes. The solution gradually became homogenous. The argon and HCl gas lines were removed and the solution was refluxed for 4 h. The solution was cooled and then concentrated under reduced pressure. The crude material was redissolved in 100 mL methanol and diethyl ether was added until a precipitate formed. The precipitate was filtered off, washed with diethyl ether, and dried in vacuo overnight to give 1 (20 g, 95%) as a white solid. MS: APCI (AP+): 146 (M)+.

Aufarbeitung

  1. custombefore bubbling in HCl gas for 15 minutes
  2. customThe argon and HCl gas lines were removed
  3. temperaturethe solution was refluxed for 4 h
  4. temperatureThe solution was cooled
  5. concentrationconcentrated under reduced pressure
  6. dissolutionThe crude material was redissolved in 100 mL methanol
  7. additiondiethyl ether was added until a precipitate
  8. customformed
  9. filtrationThe precipitate was filtered off
  10. washwashed with diethyl ether
  11. customdried in vacuo overnight

Quellen und Nachweise

ORD-Eintrag
ord-8a3caf055f784eb4a65faa44f0b9b11a
Quelldatensatz
uspto-grants-2006_04
Patentnummer
US07030141B2

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