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Sodium Carbonate → benzyl (3R,4S)-3,4-bis(hydroxymethyl)pyrrolidine-1-carboxylate

HRID 1366459
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1366459
[NH:1]1[CH2:5][C@H:4]([CH2:6][OH:7])[C@H:3]([CH2:8][OH:9])[CH2:2]1.C([O-])([O-])=O.[Na+].[Na+].Cl[C:17]([O:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:18]>CO.O>[OH:9][CH2:8][C@H:3]1[C@@H:4]([CH2:6][OH:7])[CH2:5][N:1]([C:17]([O:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[O:18])[CH2:2]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 10340Sodium CarbonateHCID 10387Benzyl chloroformateHCID 16726851cis-Pyrrolidine-3,4-diyldimethanol

Produkt 1

HCID 66936428benzyl (3R,4S)-3,4-bis(hydroxymethyl)pyrrolidine-1-carboxylateAusbeute 23 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittel
HCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

(cis)-3,4-Pyrrolidinediyldimethanol (970 mg, 7.4 mmol) was dissolved in a mixture of MeOH (20 mL) and water (7 mL) and cooled to 0° C. Na2CO3 (1.96 g, 19 mmol) was added followed by benzyl chloroformate (1.15 mL, 8.1 mmol) and the resulting solution was stirred for 4 hours, maintaining the temperature at 0° C. The reaction was concentrated under reduced pressure to remove most of the methanol, and the remaining aqueous solution was extracted twice with EtOAc. The combined organics were washed with brine and dried over sodium sulfate before being concentrated in vacuo. RP-HPLC yielded phenylmethyl (cis)-3,4-bis(hydroxymethyl)-1-pyrrolidinecarboxylate (450 mg, 22%, 1.7 mmol). LCMS: (M+H)+: 266.1.

Aufarbeitung

  1. temperaturemaintaining the temperature at 0° C
  2. concentrationThe reaction was concentrated under reduced pressure
  3. customto remove most of the methanol
  4. extractionthe remaining aqueous solution was extracted twice with EtOAc
  5. washThe combined organics were washed with brine
  6. dry with materialdried over sodium sulfate
  7. concentrationbefore being concentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-392abbbdac69464fa1d52fc6b45cca57
Quelldatensatz
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07893056B2

Notizen zur Reaktion

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