Water → 9-(2-Hydroxyethyl)-7, 11-dioxaspiro[5,5]undecane

HRID 344004Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 344004
[OH:1][CH2:2][CH:3]1[CH2:14][CH2:13][O:12][C:6]2([CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]2)[O:5][CH2:4]1.C1(C)C=CC(S(O)(=O)=O)=CC=1.O>C1C=CC=CC=1>[OH:12][CH2:13][CH2:14][CH:3]1[CH2:2][O:1][C:6]2([CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]2)[O:5][CH2:4]1

Komponenten

5

Edukt 3

HCID 962WaterHCID 6101p-Toluenesulfonic acidHCID 110308447,12-Dioxaspiro[5.6]dodecane-9-methanol

Produkt 1

HCID 108673469-(2-Hydroxyethyl)-7, 11-dioxaspiro[5,5]undecane

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel

Versuchsvorschrift

A solution of 9-hydroxymethyl-7,12-dioxaspiro[5,6]dodecane of the formula V (4 g) of the drawings in benzene (15 ml) was stirred at 10° C. for 5 hr with anhydrous p-toluenesulphonic acid (0.2 g). The reaction mixture was made alkaline by adding TEA and water. The benzene layer was separated and the aqueous layer extracted with benzene. The combined benzene solution was dried over K2CO3 and evaporate to a residue (4 g). It was chromatograped on silicagel using chloroform-methanol mixture as eluent to give 9-(2-hydroxyethyl)-7, 11-dioxaspiro[5,5]undecane of formula VI (2.8 g) (70%) of the drawings as colorless viscous liquid.

Aufarbeitung

  1. customThe benzene layer was separated
  2. extractionthe aqueous layer extracted with benzene
  3. dry with materialThe combined benzene solution was dried over K2CO3
  4. customevaporate to a residue (4 g)

Quellen und Nachweise

ORD-Eintrag
ord-c6656e9d37574e06bc52b4933d3a31c4
Quelldatensatz
uspto-grants-1999_01
Patentnummer
US05864046

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