Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50102Erstellt: 24. Oktober 2026

Toluene → HCID 178500902, Verbindung

https://huagongshe.com/de/reaction/50102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
Edukt4-FluorobenzonitrileHCID 14517—
EduktTin tetrachlorideHCID 24287—
EduktMethyl 4-methyl-3-oxopentanoateHCID 2759969—
LösungsmittelHexaneHCID 8058—
ProduktHCID 178500902HCID 17850090275,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

75.09 g of methyl isobutyrylacetate (0.50 mol, concentration 96%) and 61.80 g of 4-fluorobenzonitrile (0.50 mol, concentration 98%) were introduced into [500 ml of toluene and treated with 144.7 g of tin tetrachloride (0.55 mol, concentration 99%) at room temperature over the course of 16 min. After half an hour at room temperature, the thick suspension was heated to 80° C. After. 3 h, 175 ml of toluene were distilled off at normal pressure, and the mixture was cooled to room temperature and treated with 450 ml of saturated sodium carbonate and 300 ml of ethyl acetate. The organic phase was separated off and the aqueous phase (after dilution with 300 ml of water) was again extracted with 300 ml of ethyl acetate. After drying the combined organic phases over sodium sulphate, the solvent was removed in vacuo (40° C./25 mbar). 127.2 g of crude product were obtained in the form of a slightly yellowish solid, which was dissolved in 160 ml of n-hexane (slightly turbid solution). After hot filtration and subsequent cooling in an ice bath, 99.8 g of methyl 2-[1-amino-1-(4-fluorophenyl)-methylene]-4-methyl-3-oxopentanoate were obtained after filtration in the form of a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710178B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-1f1b485b281146ec8dd6dd9e597da9cf
Quellennotizuspto-grants-2004_03