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Acetic Acid → Tert-butyl 1-{2-[4-(methoxycarbonyl)phenyl]ethyl}-5-oxo-d-prolinate

HRID 1178557
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1178557
[NH2:1][C@@H:2]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:3][CH2:4][C:5](=[O:11])OC(C)(C)C.[C:19]([C:23]1[CH:28]=[CH:27][C:26]([CH2:29][CH:30]=O)=[CH:25][CH:24]=1)([O:21][CH3:22])=[O:20].C(O)(=O)C.[BH3-]C#N.[Na+]>CO.CCOC(C)=O>[CH3:22][O:21][C:19]([C:23]1[CH:28]=[CH:27][C:26]([CH2:29][CH2:30][N:1]2[C:5](=[O:11])[CH2:4][CH2:3][C@@H:2]2[C:12]([O:14][C:15]([CH3:16])([CH3:17])[CH3:18])=[O:13])=[CH:25][CH:24]=1)=[O:20]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 176Acetic AcidHCID 5003444Sodium cyanoborohydrideHCID 7019734Di-tert-butyl (R)-2-aminopentanedioateHCID 13844675Methyl 4-(2-oxoethyl)benzoate

Produkt 1

HCID 69250876Tert-butyl 1-{2-[4-(methoxycarbonyl)phenyl]ethyl}-5-oxo-d-prolinateAusbeute 75 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittel
HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

To a solution of H-D-Glu(OtBu)-OtBu, commercially available from Bache (0.5 g, 2.23 mmol) in MeOH (15 mL) were added 4-carbomethoxyphenylacetaldehyde (obtained from methyl 4-formyl benzoate as described in Nair et al., 1989) (0.4 g, 2.23 mmol), acetic acid (0.15 mL, 2.67 mmol), and NaCNBH3 (3.3 mL, 1.0 M THF solution, 3.3 mmol). The resulting solution was stirred at RT for 3 h then was diluted with EtOAc (100 mL) and washed with water (50 mL), and brine (50 mL). The organic solution was dried over sodium sulfate and concentrated in vacuo. The crude oil was diluted with xylene and the solution refluxed for 5 h. This solution was concentrated under reduced pressure and purified by silica gel column chromatography using EtOAc/hexane as eluent to afford the title compound (0.75 g, 75%) as a white solid. Rj 0.45 (EtOAc/hexane 1/1); 1H NMR (CDCl3) δ 1.47 (s, 9H), 1.95-2.05 (m, 1H), 2.10-2.20 (m, 1H), 2.25-2.35 (m, 1H), 2.40-2.50 (m, 1H), 2.80-3.00 (m, 2H), 3.10-3.20 (m, 1H), 3.82 (dd, 1H), 3.91 (s, 3H), 3.90-4.01 (m, 1H), 7.25 (d, 2H), 7.96 (d, 2H).

Aufarbeitung

  1. washwashed with water (50 mL), and brine (50 mL)
  2. dry with materialThe organic solution was dried over sodium sulfate
  3. concentrationconcentrated in vacuo
  4. additionThe crude oil was diluted with xylene
  5. temperaturethe solution refluxed for 5 h
  6. concentrationThis solution was concentrated under reduced pressure
  7. custompurified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-cf0abaa5498f49baa16edd46e0e63997
Quelldatensatz
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07276531B2

Notizen zur Reaktion

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