1-Bromohexane → HCID 11732181, Verbindung

HRID 1636038Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1636038
[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

3

Versuchsvorschrift

2,7-Dichloro-9,9-di(1-hexyl)fluorene is 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 shows that the sample is 99 percent or greater pure and the spectral data confirms the title structure.

Aufarbeitung

  1. customas colorless crystals (recrystallized from hexane) in 91 percent yield, melting point 66° C. to 67° C

Quellen und Nachweise

ORD-Eintrag
ord-e97e58c362204502aad03bd49c8da69e
Quelldatensatz
uspto-grants-2003_01
Patentnummer
US06512083B1

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