3-Hydroxycycloheptanone → Cycloheptane-1,3-dione
反応式
[OH:1][CH:2]1[CH2:8][CH2:7][CH2:6][CH2:5][C:4](=[O:9])[CH2:3]1>CC(C)=O>[C:4]1(=[O:9])[CH2:5][CH2:6][CH2:7][CH2:8][C:2](=[O:1])[CH2:3]1参加物
実験手順
To a 10°-20° C. solution of 20 g. (0.156 mole) of 3-hydroxycycloheptanone in 700 ml. of acetone was slowly added 54.9 ml. of 2.67M Jone's reagent (0.146 mole). The mixture was stirred 15 minutes and then quenched by addition of 12 ml. of isopropanol. The reactlon was filtered through diatomaceous earth and the filtrate concentrated on a rotovapor to about 100 ml. The residue was diluted with 300 ml. of saturated sodium chloride and then extracted with six 250 ml. portions of ether. The combined organic extract was washed with two 100 ml. portions of saturated sodium bicarbonate, dried over magnesium sulfate and evaporated under reduced pressure (aspirator) to yield an oil. Distillation of the crude oil gave 11.5 g. (58%) of the title compound as an oil.
後処理
- customTo a 10°-20° C.
- customquenched by addition of 12 ml
- filtrationThe reactlon was filtered through diatomaceous earth
- concentrationthe filtrate concentrated on a rotovapor to about 100 ml
- additionThe residue was diluted with 300 ml
- extractionof saturated sodium chloride and then extracted with six 250 ml
- extractionThe combined organic extract
- washwas washed with two 100 ml
- dry with materialportions of saturated sodium bicarbonate, dried over magnesium sulfate
- customevaporated under reduced pressure (aspirator)
- customto yield an oil
- distillationDistillation of the crude oil
- customgave 11.5 g
出典と根拠
- ORDレコード
- ord-91951afab58540e2a04d31c977361f18
- 出典データセット
- uspto-grants-1990_05
- 特許番号
- US04921994
反応ノート
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