1,3-Propanediol → gamma-Propanol

HRID 443660Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 443660
[CH2:1](O)[CH2:2][CH2:3][OH:4].[C:6]([C:10]1[CH:11]=[C:12](CCCCCCO)[CH:13]=[C:14]([C:17]([CH3:20])([CH3:19])[CH3:18])[C:15]=1[OH:16])([CH3:9])([CH3:8])[CH3:7]>>[C:6]([C:10]1[CH:11]=[C:12]([CH2:1][CH2:2][CH2:3][OH:4])[CH:13]=[C:14]([C:17]([CH3:20])([CH3:18])[CH3:19])[C:15]=1[OH:16])([CH3:7])([CH3:9])[CH3:8]

Komponenten

3

Edukt 2

HCID 104421,3-PropanediolHCID 211993774-(6-Hydroxyhexyl)-2,6-di-t-butylphenol

Produkt 1

HCID 169766gamma-PropanolAusbeute 35,5 %

Versuchsvorschrift

Substitution of 38 grams (0.5 moles) of 1,3-propanediol for the 1,6-hexanediol of Example 3 and heating the mixture for 5 hours yielded after workup 9.4 grams (35.5% yield) of 3-(3,5-di-tert.-butyl-4-hydroxyphenyl) propanol. The product is a pale yellow oil of a boiling point 135°-140° C. at 0.15 mm. of mercury which crystallized on standing to give a solid with a melting point of 67.5 to 69° C.

Quellen und Nachweise

ORD-Eintrag
ord-147a10f0ed8a45ecb1e04dcdafcbd503
Quelldatensatz
uspto-grants-1981_04
Patentnummer
US04260832

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