Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 445005Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4-(9-Methoxycarbonyl nonylsulfanyl) benzoic acid

https://huagongshe.com/reaction/445005

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium ChlorideHCID 5234—
EduktDiisopropylethylamineHCID 81531—
Edukt4-Mercaptobenzoic acidHCID 95738—
EduktMethyl 10-bromodecanoateHCID 554079—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-(9-Methoxycarbonyl nonylsulfanyl) benzoic acidHCID 66724630100%

Reaktionsschritte

4-Mercaptobenzoic acid (2.0 g, 13 mmol) was placed in THF (25 ml). DIEA (3.7 g, 28.5 mmol) was added followed by a solution of methyl 10-bromodecanoate (3.44 g, 13 mmol) in THF (10 ml). After 1 h the solvent was removed under vacuum to yield a slurry, which was stored at rt for 3 days. AcOEt (100 ml) and 1 N HCl (50 ml) were added, but the precipitate did not dissolve very well. Sat. NaCl was added and then methanol in order to aid phase separation. The aqueous phase was removed, and DCM was added to the organic phase, but the precipitates still did not dissolve. The organic phase was concentrated under vacuum and dried with toluene by adding and evaporating twice. Drying under vacuum yielded a white solid (4.4 g, quantitative yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476228B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-faec2b1b3e824bea88a82848e212668e
Quellennotizuspto-grants-2013_07