1-Bromohexane → HCID 11732181, Verbindung

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Reaktionsgleichung

[Cl:1][C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][C:8]([Cl:15])=[CH:9][CH:10]=3)[CH2:5][C:4]=2[CH:3]=1.Br[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22]>>[Cl:1][C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][C:8]([Cl:15])=[CH:9][CH:10]=3)[C:5]([CH2:13][CH2:14][CH2:2][CH2:3][CH2:4][CH3:12])([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[C:4]=2[CH:3]=1

Komponenten

Edukt 2

HCID 81011-Bromohexane

HCID 2519872,7-Dichlorofluorene

Produkt 1

HCID 11732181HCID 11732181, VerbindungAusbeute 91 %

Versuchsvorschrift

2,7-Dichloro-9,9-di(1-hexyl)fluorene was prepared from 2,7-dichlorofluorene and 1-bromohexane following the procedure of Example 1 as colorless crystals (recrystallized from hexane) in 91 percent yield; melting point 66° C. to 67° C. HPLC analysis showed that the sample was 99 percent or greater pure and the spectral data confirmed the title structure.

Aufarbeitung

customas colorless crystals (recrystallized from hexane) in 91 percent yield

Quellen und Nachweise

ORD-Eintrag: ord-bd4e6e0bae9645c884e904a094426c86
Quelldatensatz: uspto-grants-1998_01
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US05708130

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