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Water → p-Nitrobenzyl 2-(4-Ethylthio-2-oxo-1-azetidinyl)-2-(ethoxythiocarbonylthio)acetate

HRID 2291000
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2291000
[O:1]([CH2:5][CH3:6])[C:2]([S-:4])=[S:3].[K+].O.[CH2:9]([S:11][CH:12]1[N:15]([CH:16](Cl)[C:17]([O:19][CH2:20][C:21]2[CH:26]=[CH:25][C:24]([N+:27]([O-:29])=[O:28])=[CH:23][CH:22]=2)=[O:18])[C:14](=[O:31])[CH2:13]1)[CH3:10]>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.ClCCl>[CH2:9]([S:11][CH:12]1[N:15]([CH:16]([S:3][C:2]([O:1][CH2:5][CH3:6])=[S:4])[C:17]([O:19][CH2:20][C:21]2[CH:22]=[CH:23][C:24]([N+:27]([O-:29])=[O:28])=[CH:25][CH:26]=2)=[O:18])[C:14](=[O:31])[CH2:13]1)[CH3:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 962WaterHCID 2735045Potassium ethylxanthateHCID 14050378p-Nitrobenzyl 2-(4-ethylthio-2-oxo-1-azetidinyl)-2-chloroacetate

Produkt 1

HCID 54336749p-Nitrobenzyl 2-(4-Ethylthio-2-oxo-1-azetidinyl)-2-(ethoxythiocarbonylthio)acetate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 66133Benzyl triethylammonium chloride
Katalysator
HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a stirred mixture of 3.2 g. of potassium ethyl xanthate, 5.4 g. of benzyltriethylammonium chloride, 100 ml. of water and 50 ml. of dichloromethane, at 0° C., was added a solution of 7.12 g. of p-nitrobenzyl 2-(4-ethylthio-2-oxo-1-azetidinyl)-2-chloroacetate in 75 ml. of dichloromethane. Stirring was continued at 0°-5° C. for 1 hour, and then the organic phase was removed. The aqueous phase was extracted with 100 ml. of dichloromethane, and then the combined dichloromethane layers were washed successively with 75 ml. of dilute hydrochloric acid, 75 ml. of saturated aqueous sodium bicarbonate and 75 ml. of water. The dichloromethane solution was dried with anhydrous sodium sulfate and evaporated to dryness in vacuo, and the residue was purified by column chromatography on 200 g. of silica gel, eluting with 95:5 chloroform-ethyl acetate. The product containing fractions were combined and concentrated in vacuo to give 4.3 g of the title compound. The IR spectrum (chloroform) showed an absorption at 5.66 microns. The NMR spectrum (deuterochloroform) showed peaks at 1.02-1.6 (m, 6H); 2.35-3.65 (m, 4H); 4.4-5.1 (m, 3H); 5.3 (s, 2H); 6.3 and 6.4 (ss, 1H); 7.4 (d, 2H); and 8.2 (d, 2H) ppm.

Aufarbeitung

  1. additionTo a stirred mixture of 3.2 g
  2. customthe organic phase was removed
  3. extractionThe aqueous phase was extracted with 100 ml
  4. washof dichloromethane, and then the combined dichloromethane layers were washed successively with 75 ml
  5. dry with materialThe dichloromethane solution was dried with anhydrous sodium sulfate
  6. customevaporated to dryness in vacuo
  7. customthe residue was purified by column chromatography on 200 g
  8. washof silica gel, eluting with 95:5 chloroform-ethyl acetate
  9. additionThe product containing fractions
  10. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-4dba25f2e84d4c5eb4aea2ab6f0bc5ab
Quelldatensatz
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04619783

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