Hydrochloric Acid → 4-Hydroxymethyl-1-methyl-1-cyclohexanecarboxylic acid
反応式
[OH-].[Na+].[OH:3][CH2:4][CH:5]1[CH2:10][CH2:9][C:8]([CH3:15])([C:11]([O:13]C)=[O:12])[CH2:7][CH2:6]1.Cl>CO>[OH:3][CH2:4][CH:5]1[CH2:10][CH2:9][C:8]([CH3:15])([C:11]([OH:13])=[O:12])[CH2:7][CH2:6]1参加物
実験手順
50 ml of 3N aqueous sodium hydroxide solution was added to a solution of 4.5 g of methyl 4-hydroxymethyl-1-methyl-1-cyclohexanecarboxylate (Example 42) in 100 ml of methanol. The solution was reacted for 2 hours, while it was refluxed. After reaction, 2N hydrochloric acid was added to the reaction solution, acidifying the solution. The solution was extracted five times with 50 ml of ethyl acetate. The organic layer obtained was washed three times with an aqueous sodium chloride solution and dried over magnesium sulfate. Thereafter, the solvent was removed in vacuo. The oily substance obtained was subjected to column chromatography using 50 g of silica gel. From the fraction eluted with hexane and ethyl acetate=1:1, the solvent was removed in vacuo, yielding 2.5 g of 4-hydroxymethyl-1-methyl-1-cyclohexanecarboxylic acid as a pale yellow oily, which had the following physiochemical properties:
後処理
- customThe solution was reacted for 2 hours, while it
- temperaturewas refluxed
- additionwas added to the reaction solution
- extractionThe solution was extracted five times with 50 ml of ethyl acetate
- customThe organic layer obtained
- washwas washed three times with an aqueous sodium chloride solution
- dry with materialdried over magnesium sulfate
- customThereafter, the solvent was removed in vacuo
- customThe oily substance obtained
- washFrom the fraction eluted with hexane and ethyl acetate=1:1
- customthe solvent was removed in vacuo
出典と根拠
- ORDレコード
- ord-141228f0cbc343b0888c36b8da1cda70
- 出典データセット
- uspto-grants-1994_09
- 特許番号
- US05344845
反応ノート
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