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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1885389Erstellt: 26. Oktober 2026

Dimethyl Sulfide → 2-Methyl-1-phenyl-1-propanol

https://huagongshe.com/reaction/1885389

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfideHCID 1068—
EduktTriglymeHCID 8189—
EduktEthyl sulfideHCID 9609—
EduktPhenylpropanolamine HydrochlorideHCID 62943—
EduktIsobutyrophenoneHCID 69144—
Edukt(E)-1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)-4,4-dimethyl-1-penten-3-oneHCID 11110117—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelChlorobenzeneHCID 7964—
Produkt2-Methyl-1-phenyl-1-propanolHCID 9562697,2%

Reaktionsschritte

The same procedure as in Example 1 was repeated except that (+)-norephedrine hydrochloride was replaced by (-)-norephedrine hydrochloride, triglyme was replaced by 0.4 ml of dimethylformamide, dimethyl sulfide was replaced by diethyl sulfide, monochlorobenzene was replaced by 1,2-dichloroethane, (E)-1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)-4,4-dimethyl-1-penten-3-one was replaced by 0.27 g (1.85 mmoles) of phenyl isopropyl ketone, and the reduction reaction was conducted for 18.5 hours, to obtain 0.27 g of crude (-)-phenylisobutyl alcohol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05144039
Quelldatensatzuspto-grants-1992_09
ORD IDord-ac302dae37ed47baba21ba0f22a696a4
Quellennotizuspto-grants-1992_09