Reaktion #59923

ord-3eddc8993b914b09824dff92265f7283

Reaktionsgleichung

CCCC1(CCO)OCCCO1
( 8b )
CCCC1(CCO)OCCCO1
2-(2-propyl-1,3-dioxan-2-yl)ethanol
CCOC(=O)CC(C)=O
ethyl acetoacetate
CC(C)(CO)CO
2,2-dimethyl-1,3-propanediol
CC1(C)COC(C)(CCO)OC1
title compound
Ausbeute 55.0%
CC1(C)COC(C)(CCO)OC1
2-(2,5,5-trimethyl-1,3-dioxan-2-yl)ethanol
Ausbeute 55.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The same procedure as in the steps (8a) and (8b) of Example 8 was repeated using ethyl acetoacetate, and 2,2-dimethyl-1,3-propanediol to obtain the title compound (7.3 g, total yield: 55%) as a light yellow oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07425634B2uspto-grants-2008_09