反応 #56252
ord-b1f1db6c8eae432a8215007ed7a4411a
反応方程式
反応条件
後処理
- 1その他are passed into the mixture at 20°-30° C
- 2workup.DISSOLUTIONdissolves
- 3温度The mixture is cooled in a water bath
- 4workup.STIRRINGwith stirring
- 5workup.ADDITIONto rise to about 50° C. during the alkali addition
- 6その他to remove as much tetrahydrofuarn as possible
- 7その他A solid precipitates
- 8温度while heating
- 9workup.ADDITIONof water are added
- 10温度the entire mixture is cooled to about 10° C. in an ice bath
- 11ろ過The solid is filtered
- 12洗浄washed with water
- 13その他pulled dry
- 14その他The cake is recrystallized from 800 ml
- 15その他boiling isopropanol refrigerated overnight
- 16ろ過The crystals are filtered
- 17洗浄washed with cold isopropanol
- 18その他dried at about 100° C
実験手順
360 ml. of tetrahydrofuran is combined with 90 gm. of crotonaldehyde and placed in an ice bath. 100 gm. of hydrogen chloride are passed into the mixture at 20°-30° C. 158 gm. of 5-chlorosalicylhydroxamic acid is added in one portion and the mixture stirred at 25°-30° C. for about two hours until the solid dissolves. The mixture is cooled in a water bath and 400 ml. of concentrated ammonium hydroxide diluted with 400 ml. of water is added with stirring. The temperature of the mixture is allowed to rise to about 50° C. during the alkali addition and the mixture is then heated on a steam bath to about 90° C. and a vacuum applied to remove as much tetrahydrofuarn as possible. A solid precipitates while heating. 400 ml. of water are added and the entire mixture is cooled to about 10° C. in an ice bath. The solid is filtered and washed with water and pulled dry. The cake is recrystallized from 800 ml. boiling isopropanol refrigerated overnight. The crystals are filtered, washed with cold isopropanol and dried at about 100° C. 136 gm. 7-chloro-2-methyl-3,3a-dihydro-2H, 9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one (m.p. 144°-148° C.) for a yield of 67% is obtained.