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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18065Erstellt: 24. Oktober 2026

Sodium methanesulfinate → Methyl 5-(methylsulfonylmethyl)thiophene-2-carboxylate

https://huagongshe.com/de/reaction/18065

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium methanesulfinateHCID 2733271—
EduktMethyl 5-(bromomethyl)thiophene-2-carboxylateHCID 11424851—
LösungsmittelEthanolHCID 702—
ProduktMethyl 5-(methylsulfonylmethyl)thiophene-2-carboxylateHCID 1790844429,4%

Reaktionsschritte

Methyl 5-(methylsulfonylmethyl)thien-2-ylcarboxylate may be obtained in the following manner: 31.7 g of sodium methyl sulfinate are added to a solution of 73 g of methyl 5-(bromomethyl)thien-2-ylcarboxylate in 150 cm3 of ethanol and the suspension obtained is heated under reflux for 7 hours. The reaction medium is then concentrated to dryness under reduced pressure (2.7 kPa). The residue is extracted with four times 500 cm3 of ethyl acetate, the combined organic phases are washed successively with 250 cm3 of distilled water and 250 cm3 of a saturated sodium chloride solution, dried over magnesium sulfate, filtered and incompletely concentrated under reduced pressure. The solid which appears is isolated by filtration, rinsed with three times 25 cm3 of ice-cold ethyl acetate and provides 21.4 g of methyl 5-(methylsulfonylmethyl)thien-2-ylcarboxylate in the form of a cream-colored powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741316B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-1ff1cf8dc3044664b62f6f776d19baa5
Quellennotizuspto-grants-2010_06