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Hexane → 3-Thiophenecarboxylic acid, tetrahydro-4-oxo-, methyl ester

HRID 902505
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 902505
[CH3:1][O:2][C:3](=[O:12])[CH2:4][CH2:5][S:6][CH2:7][C:8](OC)=[O:9].CCCCCC.[H-].[Na+]>C1COCC1>[CH3:1][O:2][C:3]([CH:4]1[C:8](=[O:9])[CH2:7][S:6][CH2:5]1)=[O:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8058HexaneHCID 24758Sodium hydrideHCID 81891Propanoic acid, 3-((2-methoxy-2-oxoethyl)thio)-, methyl ester

Produkt 1

HCID 984243-Thiophenecarboxylic acid, tetrahydro-4-oxo-, methyl esterAusbeute 35,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of 3-methoxycarbonylmethylsulfanyl-propionic acid methyl ester (32) (58 g, 300 mmol) in dry T HF (800 mL) was added slowly within 4 h to a refluxing solution of hexane washed NaH (60% in mineral oil, 13.24 g, 331 mmol) in THF. The solution was further refluxed for 5 h. The solution was cooled and the solvent was evaporated. The residue was taken in water, acidified to pH˜1 by cold HCl solution, and extracted by CH2Cl2. The combined organic phase was dried over MgSO4 and concentrated under vacuum to get a viscous residue. The residue was purified by flash chromatography eluting with hexane to yield 17 g (35%) of 4-oxo-tetrahydro-thiophene-3-carboxylic acid methyl ester as colorless viscous oil which solidified on keeping overnight under vacuum. MP 51° C.; 1H NMR (400 MHz, CDCl3) δ 3.17-3.82 (m, 6.5 H), 10.94 (s, 0.5H) ppm. The isomeric mixture was used to next step without further purification.

Aufarbeitung

  1. temperatureThe solution was further refluxed for 5 h
  2. temperatureThe solution was cooled
  3. customthe solvent was evaporated
  4. extractionextracted by CH2Cl2
  5. dry with materialThe combined organic phase was dried over MgSO4
  6. concentrationconcentrated under vacuum
  7. customto get a viscous residue
  8. customThe residue was purified by flash chromatography
  9. washeluting with hexane

Quellen und Nachweise

ORD-Eintrag
ord-66827354dd654637a18276becefa3c17
Quelldatensatz
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07365200B2

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