Cyclohexanol → 4-(Bromomethyl)cyclohexan-1-ol

HRID 1289348Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1289348
[CH:1]1([OH:7])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Br:8][CH2:9]C1(O)CCCCC1.COC1CCC(C(O)=O)CC1>>[Br:8][CH2:9][CH:4]1[CH2:5][CH2:6][CH:1]([OH:7])[CH2:2][CH2:3]1

Komponenten

4

Versuchsvorschrift

Modified polyvinylbutryal containing a pendant group with cyclohexanol was prepared by the reaction of PVB with tetrahydropyranyl (THP) protected bromomethylcyclohexanol, followed by acid hydrolysis of the THP protection group. The THP-protected cyclohexanol-containing moiety was prepared by the following reaction sequence: 4-Methoxycyclohexanoic acid was reduced with borane-tetrahydrofuran complex to obtain 4-bromomethyl-cyclohexanol. This compound was treated with phosphorus tribromide to obtain the corresponding bromo compound. This bromo compound was reacted with trimethylsilyliodide to cleave the methoxy group to obtain 4-bromomethyl-cyclohexanol, which in turn was treated with dihyhdropyran to obtain the tetrahydropyranyl-protected bromomethylcyclohexanol. This preparation is represented by the following reaction scheme and further described in paragraphs a-d below. ##STR3## a) Preparation of 4-bromomethylcyclohexanol (C-3)

Aufarbeitung

  1. customwas prepared by the reaction of PVB with tetrahydropyranyl (THP)
  2. customwas prepared by the following reaction sequence

Quellen und Nachweise

ORD-Eintrag
ord-78c9071ac414486f9393e4b9e93d513a
Quelldatensatz
uspto-grants-1998_05
Patentnummer
US05750300

Notizen zur Reaktion

Wird geladen…