反応式
[OH-:1].[K+].[O:3]1[CH2:7][CH2:6][CH2:5][CH2:4]1.O>O>[CH:6]12[CH2:7][CH:4]([CH:4]=[CH:5]1)[CH2:5][CH:6]2[C:7]([OH:3])=[O:1]参加物
4
実験手順
67.0 g (269 mmol) of the Diels-Alder adduct was dissolved in 1040 ml of a mixture solvent of tetrahydrofuran-water (5:2), 70.5 g (1.08 mol) of potassium hydroxide (85%) in 300 ml of water was added on ice cooling, and the mixture was stirred at room temperature for 24 hours. After distilling out tetrahydrofuran, the product was neutralized with 94 ml of concentrated hydrochloric acid and extracted with a mixture solvent of hexane-methylene chloride (98:2) (200 ml×4). The extract was dried on anhydrous magnesium sulfate, the solution was filtered, and the solvent was distilled off to obtain 38.8 g of crude 5-norbornene-2-carboxylic acid. Crude yield: 100%.
後処理
- additionwas added on ice cooling
- distillationAfter distilling out tetrahydrofuran
- extractionextracted with a mixture solvent of hexane-methylene chloride (98:2) (200 ml×4)
- dry with materialThe extract was dried on anhydrous magnesium sulfate
- filtrationthe solution was filtered
- distillationthe solvent was distilled off
出典と根拠
- ORDレコード
- ord-5b97708d54a6469088360f4acddde66a
- 出典データセット
- uspto-grants-1993_11
- 特許番号
- US05266728
関連ノート
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