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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1194564Erstellt: 25. Oktober 2026

Butanethiol → 6-(6-Hydroxy-2-naphthyl)-6-oxohexanoic acid

https://huagongshe.com/reaction/1194564

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButanethiolHCID 8012—
EduktDibutyl sulfideHCID 11002—
EduktButyl methyl sulfideHCID 12339—
EduktSodium hydrideHCID 24758—
Edukt6-(6-Methoxy-2-naphthyl)-6-oxo-hexanoic acidHCID 14425905—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-(6-Hydroxy-2-naphthyl)-6-oxohexanoic acidHCID 1398254179%

Reaktionsschritte

Butyl sulfide was generated by placing NaH (2.57 g, 0.11 mol) in a 500 ml round bottom flask, adding butanethiol (5.14 ml, 0.48 mol) and stirring for 5 minutes. DMF (200 mls) was added and the reaction heated at reflux. Slowly, 6-(6-methoxy-2-naphthyl)-6-oxo-hexanoic acid (Example 5) (7.2 g, 0.25 mol) in DMF (100 ml) was added to the reaction and heated at reflux for 1 hour. The methyl butyl sulfide and DMF were vacuum distilled (7 torr, 28° C.) to leave a bright yellow powder that was dissolved in water and precipitated with 5% HCl. The precipitate was filtered, dissolved in ethyl acetate (1800 ml), dried (Na2SO4), filtered and evaporated to give a yellow solid that was recrystallized (ethyl acetate) to give the title compound (5.38 grams, 79% yield), mp 191°-193° C.; MS, m/e 272 (M+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04814487
Quelldatensatzuspto-grants-1989_03
ORD IDord-b3caeb6368f84277bd04656f9db1ea14
Quellennotizuspto-grants-1989_03