反応 #3712

ord-170e488e116e4e0492b95134d1d42168

反応方程式

O=C1CCCC(=O)C1
cyclohexane-1,3-dione
CC(C)(CO)CO
2,2-dimethylpropane-1,3-diol
CC1(C)COC2(CCCC(=O)C2)OC1
3,3-dimethyl-1,5-dioxa-spiro[5,5]undecan-8-one

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

125 g (630 mmole) 3,3-dimethyl-1,5-dioxa-spiro[5,5]undecan-8-one, which was obtained by the azeotropic acetylation of cyclohexane-1,3-dione with 2,2-dimethylpropane-1,3-diol in toluene as a solvent using p-toluenesulphonic acid as a catalyst, and 59 g (630 mmole) dimethylammonium methylene chloride were stirred at room temperature in 400 ml of dry acetonitrile. After adding 1 ml acetyl chloride the mixture was stirred for a further 3 hours at room temperature, whereupon a clear colourless solution was obtained. 800 ml of dry ether were then added drop-wise to the reaction mixture, whereupon the hydrochloride crystallised out. 158 g of (18) were obtained (98% theoretical).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05733936uspto-grants-1998_03