Formaldehyde → Bis(3-phenyl-2-indenyl)methane

HRID 2121098

Reaktionsgleichung

[C:1]1([CH:7]2[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[CH:9]=[CH:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C=O.[C:18]1([CH3:28])[CH:23]=[CH:22][C:21](S(O)(=O)=O)=[CH:20][CH:19]=1>C1(C)C=CC=CC=1>[C:1]1([C:7]2[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[CH2:9][C:8]=2[CH2:9][C:8]2[CH2:28][C:18]3[C:23]([C:7]=2[C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Komponenten

Reaktionsbedingungen

Temperatur: 80 °C

Versuchsvorschrift

In a 500 mL flask equipped with magnetic stirring bar were introduced 4.46 g (0.023 moles) of 1-phenyl-indene, 0.35 g (0.0117 moles) of formalin and 0.88 g (0.0046 moles) of para-toluenesulphonic acid in 200 ml of toluene; the mixture was heated to 80° C. and was maintained under stirring for 6 hours at 80° C. Then the reaction was quenched with water/NaHCO3; the organic layer was separated, washed with water and brought to dryness under reduced pressure. The crude product was crystallized upon standing at room temperature, and then was further purified by washing with pentane or MeOH, thus isolating 4.5 g of bis(3-phenyl-2-indenyl)methane (purity of 97.3% by G.C.; yield=95.2%).

Aufarbeitung

customIn a 500 mL flask equipped with magnetic stirring bar
temperaturewas maintained
customThen the reaction was quenched with water/NaHCO3
customthe organic layer was separated
washwashed with water
customThe crude product was crystallized
customupon standing at room temperature
customwas further purified
washby washing with pentane or MeOH

Quellen und Nachweise

ORD-Eintrag: ord-82df646569fa474eb94813285ba91a8c
Quelldatensatz: uspto-grants-2004_02
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US06693156B1

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