Reaktion #1552674

ord-f0cd830b6a464893a0c491d09d6d9129

Reaktionsgleichung

COC(=O)c1ccc(CO)s1
methyl 5-(hydroxymethyl)thiophene-2-carboxylate
O=S(Cl)Cl
thionyl chloride
COC(=O)c1ccc(CCl)s1
methyl 5-(chloromethyl)thiophene-2-carboxylate
Ausbeute 111.8%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthe mixture was concentrated under reduced pressure
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in anhydrous chloroform (10 ml)
  3. 3
    Einengenthe mixture was concentrated again under reduced pressure
  4. 4
    Sonstigeto remove thionyl chloride azeotropically
  5. 5
    SonstigeThe residue was dried under reduced pressure

Vorschrift

To a solution of methyl 5-(hydroxymethyl)thiophene-2-carboxylate (1.440 g, 8.362 mmol) in anhydrous chloroform (7.5 ml) was added dropwise thionyl chloride (3.62 ml, 50.17 mmol) at 0° C. After stirring at room temperature for 1.5 hrs, the mixture was concentrated under reduced pressure. The residue was dissolved in anhydrous chloroform (10 ml), and the mixture was concentrated again under reduced pressure. This operation was repeated 3 times to remove thionyl chloride azeotropically. The residue was dried under reduced pressure to give crude methyl 5-(chloromethyl)thiophene-2-carboxylate (1.782 g) as a brown oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08999989B2uspto-grants-2015_04