Technology Process of 2-Cyclohexen-1-one, 3-(trimethylstannyl)-
There total 2 articles about 2-Cyclohexen-1-one, 3-(trimethylstannyl)- which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
In
tetrahydrofuran;
a cold (-20°C) stirred soln. of the cuprate reagent was allowed to react with β-iodo enone in dry THF; the mixt. was stirred under dry Ar atm. at -20°C for 15 min and at room temp. for 30 min;; chromy. (in mixt. of methanol and diethyl ether) followed by the elution with diethyl ether; removal of the solvent by distn. (air-bath temp. 65-80°C/0.09 Torr);;
- Guidance literature:
-
In
tetrahydrofuran;
a cold (-78°C) stirred soln. of trimethylstannyl-lithium in dry THF was allowed to react with 3-iodo-2-cyclohexen-1-one in dry THF; the mixt. was stirred under dry argon atm. at -78°C for 1 h;; satd. aq. NH4Cl (pH 8) and diethyl ether were added and the mixt. was stirred for several min.; the organic layer was sepd., washed with brine and dried (MgSO4); removal of the solvent and sepn. of compds. by distn. glc anal.; elem. anal.;