반응 #94255
ord-fa605c18c67c4c4f80dcb5deb8ca8779
반응 방정식
반응물
시약
반응 조건
후처리
- 1기타round-bottomed flask was equipped with a mechanical stirrer
- 2온도reflux condenser
- 3workup.ADDITIONsurmounted by calcium chloride drying tube, addition funnel
- 4기타was placed in a water bath at 221
- 5기타2 ° C
- 6기타did not rise over 23° C
- 7기타Reaction
- 8workup.WAITthe reaction was completed after another 3 days
- 9기타was withdrawn from the reaction mixture
- 10workup.WAITto stand for 15 minutes
- 11여과The quinoline hydrochloride was filtered off
- 12세척washed with 25 ml pentane which
- 13workup.ADDITIONwas added to the pentane solution
- 14세척This solution was then successively washed with 25 ml
- 15건조portions of water, and finally dried over sodium sulfate
- 16기타After removal
- 17건조of drying agent and pentane
- 18기타was obtained
실험 절차
A four-necked 500 ml. round-bottomed flask was equipped with a mechanical stirrer, reflux condenser surmounted by calcium chloride drying tube, addition funnel and thermometer. A solution of 19 g. (0.1 mole) 1,3-dimethyl-3-(t-butylperoxy)butyl alcohol and 13.3 g (slightly over 0.1 mole) quinoline in 250 ml. pentane was placed in the flask which was placed in a water bath at 221/2 ° C. Then 12.3 g (0.1 mole) isopropyl chloroformate was added dropwise over 5 minutes; the temperature did not rise over 23° C. Reaction was not complete after 3 days. Another 3 g. of quinoline was added, and the reaction was completed after another 3 days as indicated by the fact that no further precipitate of quinoline hydrochloride formed when an aliquot of clean pentane solution was withdrawn from the reaction mixture and allowed to stand for 15 minutes. The quinoline hydrochloride was filtered off and washed with 25 ml pentane which was added to the pentane solution. This solution was then successively washed with 25 ml. of 7% hydrochloric acid, two 50 ml. portions of water, and finally dried over sodium sulfate. After removal of drying agent and pentane, a yield of 23.8 g. (86.4%) of material found to be 1,3-dimethyl-3-(t-butylperoxy)butyl isopropyl carbonate by infrared analysis, was obtained.