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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20729Erstellt: 23. Oktober 2026

3-(Methylthio)-1-propanol → 2-(3-Methylsulfanyl-propoxy)-isoindole-1,3-dione

https://huagongshe.com/de/reaction/20729

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Methylthio)-1-propanolHCID 10448—
EduktN-HydroxyphthalimideHCID 10665—
EduktTriphenylphosphineHCID 11776—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(3-Methylsulfanyl-propoxy)-isoindole-1,3-dioneHCID 5934800465,4%

Reaktionsschritte

3-Methylsulfanyl-propan-1-ol (4.133 g, 38.92 mmol) was dissolved in THF (anhydrous, 100 mL). To this solution, triphenylphosphine (10.2 g, 38.92 mmol) and N-hydroxyphthalimide (6.4 mg, 38.92 mmol) were added and dissolved with stirring. Diisopropyl azodicarboxylate (8.5 mL, 42.812 mmol) was added dropwise thereto with cooling the reaction vessel in an ice-bath under nitrogen atmosphere. The reaction mixture was warmed to room temperature, and stirred for 5 hours. After completion of the reaction, the reaction mixture was concentrated under reduced pressure, and triturated with diethyl ether:hexane (1:1, about 100 ml) to precipitate triphenylphosphine oxide as a white solid, which was filtered off. The filtrate was concentrated under reduced pressure to give a yellow oily residue. The resultant yellow oil was purified by silica gel flash chromatography (BW300, Fuji Silysia Chemical, 20% ethyl acetate/hexane as an eluent) to give 2-(3-methylsulfanyl-propoxy)-isoindole-1,3-dione (6.4 g, 65%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745663B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-da442fe9c3494a84b96c52bc1aad841c
Quellennotizuspto-grants-2010_06