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Iodine → 2-Methoxy-pyrrolidine-1-carboxylic acid benzyl ester

HRID 132819
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 132819
[CH2:1]([O:8][C:9]([N:11]1[CH2:15][CH2:14][CH2:13][C@H:12]1C(O)=O)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:19](OC1C(OC(=O)C)=C(I=O)C=CC=1)(=[O:21])C.II.CO>ClCCl>[CH2:1]([O:8][C:9]([N:11]1[CH2:15][CH2:14][CH2:13][CH:12]1[O:21][CH3:19])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 807IodineHCID 887MethanolHCID 101987Benzyloxycarbonyl-L-prolineHCID 21113495Diacetoxyiodosobenzene

Produkt 1

HCID 109224852-Methoxy-pyrrolidine-1-carboxylic acid benzyl esterAusbeute 88,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344
Dichloromethane
Lösungsmittel

Versuchsvorschrift

To a mixture of (S)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester (purchased at Fluka, Ref 97090, 6 g, 1.0 eq.) in dichloromethane (300 mL) was added diacetoxyiodosobenzene (15.8 g, 2 eq.) and iodine (3.0 eq., 0.5 eq.). The mixture was stirred 5 h at room temperature. Methanol (12 mL) was added and the reaction mixture was stirred for an additional 1.5 h at room temperature, partitioned between an aqueous solution of sodium sulfite and dichloromethane. The organic layer was washed with an aqueous solution of sodium sulfite, brine, evaporated in vacuo and purified on silica eluting with 9:1 cyclohexane/ethyl acetate to yield 5.0 g (88%) of the desired product as light yellow oil. MS (m/e): 235.5 (MH+, 100%)

Aufarbeitung

  1. stirringthe reaction mixture was stirred for an additional 1.5 h at room temperature
  2. custompartitioned between an aqueous solution of sodium sulfite and dichloromethane
  3. washThe organic layer was washed with an aqueous solution of sodium sulfite, brine
  4. customevaporated in vacuo
  5. custompurified on silica eluting with 9:1 cyclohexane/ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-b86cbbeb5da042a2aaf26fadcae3ef6d
Quelldatensatz
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07388095B2

Notizen zur Reaktion

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