Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List 1,2-Octanediol

1,2-Octanediol synthesis

7synthesis methods
1,2-Octanediol is widely used in synthetic fragrances, lubricant additives, plasticizers and adhesives. The synthetic method of 1,2-octanediol is that: add 1-octene to the mixed solution of formic acid and hydrogen peroxide, adjust the pH to distill after stirring for 100 min, collect fractions under the condition of 131°C/1330Pa, and the obtained fractions is1,2-octanediol.
-

Yield:1117-86-8 42%

Reaction Conditions:

with tert.-butylhydroperoxide;OsO4 in tert-butyl alcohol

Steps:

1 EXAMPLE 1
EXAMPLE 1 Into a 100 ml 3-neck round bottom flask equipped with a magnetic stirrer, reflux condenser, dropping funnel, and thermometer, is charged 0.025 g (0.1 mmole) OsO4, 10.1 g t-butyl alcohol, 3.0 g 1-octene, and 0.037 g (0.2 mmole) n-butyl iodide (co-catalyst I) under continuous agitation and atmospheric pressure. An aqueous solution (2.9 g) containing 70% t-butyl hydroperoxide is then added at atmospheric pressure slowly over a period of 30 minutes at 26° C. to the mixture thereby introducing a total of 22 mmoles of hydroperoxide. The total amount of water in the resulting mixture is 5.9 g. The contents of the flask are warmed to 45° C. as a result of the reaction exotherm during the addition of the hydroperoxide solution. The pH of the resulting solution is about 5. The contents of the reaction flask is then analyzed by gas chromatography upon completion of hydroperoxide addition. The conversion of hydroperoxide is found to be 100%. 1.3 g of 1,2-octanediol is obtained indicating a selectivity to glycol of 42% and a yield of 42%.

References:

Exxon Research & Engineering Co. US4482763, 1984, A

FullText

1,2-Octanediol Related Search: