2-Methyl-2-butene → 1-Methyl-4-(propan-2-yl)cyclohexane-1-carboxylic acid
反応式
[CH:1]([CH:4]1[CH2:9][CH2:8][C:7]([CH3:12])([CH:10]=[O:11])[CH2:6][CH2:5]1)([CH3:3])[CH3:2].CC(=CC)C.Cl([O-])=[O:19].[Na+].P([O-])(O)(O)=O.[Na+]>O.C(O)(C)(C)C>[CH:1]([CH:4]1[CH2:5][CH2:6][C:7]([CH3:12])([C:10]([OH:19])=[O:11])[CH2:8][CH2:9]1)([CH3:3])[CH3:2]参加物
実験手順
A flask was charged with 10 g of 4-isopropyl-1-methyl cyclohexane carbaldehyde, 200 mL of tert-butanol and 100 mL of 2-methyl-2-butene. While stirring the contents of the flask, a solution prepared by dissolving 13 g of sodium chlorite and 11 g of sodium dihydrogenphosphate in 80 mL of water was added to the flask at 0° C. After stirring the contents of the flask at room temperature for 40 min, a part of tert-butanol in the flask was distilled off, and then a small amount of sulfuric acid was added to the flask. The resulting reaction mixture was extracted with an ether, and the thus obtained extract solution was concentrated and then purified by a silica gel column, thereby obtaining 11 g of 4-isopropyl-1-methyl cyclohexanecarboxylic acid.
後処理
- customa solution prepared
- additionwas added to the flask at 0° C
- stirringAfter stirring the contents of the flask at room temperature for 40 min
- distillationa part of tert-butanol in the flask was distilled off
- additiona small amount of sulfuric acid was added to the flask
- customThe resulting reaction mixture
- extractionwas extracted with an ether
- customthe thus obtained
- extractionextract solution
- concentrationwas concentrated
- custompurified by a silica gel column
出典と根拠
- ORDレコード
- ord-4b1af3289f7b44baae2f2dd24442437d
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08383574B2
反応ノート
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