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Methanol → Methyl 1-(mercaptomethyl)cyclopropaneacetate

HRID 1986032
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1986032
[SH:1][CH2:2][C:3]1([CH2:6][C:7]([OH:9])=[O:8])[CH2:5][CH2:4]1.S(=O)(=O)(O)O.[CH3:15]O>>[CH3:15][O:8][C:7](=[O:9])[CH2:6][C:3]1([CH2:2][SH:1])[CH2:5][CH2:4]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 97938251-(Mercaptomethyl)cyclopropaneacetic acid

Produkt 1

HCID 15288152Methyl 1-(mercaptomethyl)cyclopropaneacetate

Reaktionsbedingungen

Temperatur
20.5 °C

Versuchsvorschrift

To a 3 L flask, a solution of 1-(mercaptomethyl)cyclopropaneacetic acid (330.7 g) in methanol (1500 ml) was charged. 96% sulfuric acid (36 g) was added, and the reaction mixture was stirred for 5 h at 19-22° C. The reaction mixture was concentrated to ¼ of its volume at 50° C. under reduced pressure, and the residue was partitioned between water (1000 ml) and ethyl acetate (500 ml). The organic phase was separated, washed with 10% NaHCO3 and 5% NaCl (200 ml), and dried overnight over anhydrous sodium sulfate. The mixture was filtered and evaporated at 50° C. under reduced pressure, to afford 315.7 g of the crude 1-(mercaptomethyl)cyclopropaneacetic acid methyl ester, as a colored liquid with a strong, unpleasant odor.

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated
  2. customto ¼ of its volume at 50° C. under reduced pressure
  3. customthe residue was partitioned between water (1000 ml) and ethyl acetate (500 ml)
  4. customThe organic phase was separated
  5. washwashed with 10% NaHCO3 and 5% NaCl (200 ml)
  6. dry with materialdried overnight over anhydrous sodium sulfate
  7. filtrationThe mixture was filtered
  8. customevaporated at 50° C. under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-59904bd714034c349137f9ed85d5eb68
Quelldatensatz
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07547787B2

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