Methyl 3-(2-oxoindolin-3-yl)propanoate → 3-(3-Hydroxypropyl)indolin-2-one

HRID 2363030Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2363030
[H-].[Al+3].[Li+].[H-].[H-].[H-].[O:7]=[C:8]1[CH:16]([CH2:17][CH2:18][C:19](OC)=[O:20])[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[NH:9]1>O1CCCC1>[OH:20][CH2:19][CH2:18][CH2:17][CH:16]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[NH:9][C:8]1=[O:7]

Komponenten

4

Edukt 2

HCID 14903583Methyl 3-(2-oxoindolin-3-yl)propanoateHCID 21226445Aluminium lithium hydride

Produkt 1

HCID 122442773-(3-Hydroxypropyl)indolin-2-oneAusbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Lithium aluminum hydride (0.5M solution in diglyme, 13.8 mL, 6.9 mmol) was added dropwise at 0° C. to methyl 3-(2-oxoindolin-3-yl)propanoate (1.51 g, 6.90 mmol) in tetrahydrofuran (30 mL). The mixture was allowed to warm to room temperature and then quenched with 2N aqueous hydrochloric acid. The reaction was extracted with ethyl acetate. The extract was weashed with brine, dried (MgSO4) and evaporated. The residue was purified by Biotage flash column chromatography (50% ethyl acetate/hexanes) to give product as a white solid (1.13 g, 86%); 1H NMR (DMSO-d6); δ1.38 (m, 2H); 1.85 (m, 2H); 3.32-3.38 (t, J=6.4 Hz, 1H); 4.38 (t, J=5.2 Hz, 1H); 6.80 (d, J=8 Hz, 1H); 6.94 (m, 1H); 7.16 (m, 1H); 7.22 (d, J=7.2 Hz, 1H); 10.3 (s, 2H)

Aufarbeitung

  1. customquenched with 2N aqueous hydrochloric acid
  2. extractionThe reaction was extracted with ethyl acetate
  3. dry with materialdried (MgSO4)
  4. customevaporated
  5. customThe residue was purified by Biotage flash column chromatography (50% ethyl acetate/hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-605fdc8010df452f90bec215655ee48c
Quelldatensatz
uspto-grants-2014_04
Patentnummer
US08691836B2

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