Glycolic Acid → O-(3-Acetylthiopropanoyl)glycolic Acid
反応式
[C:1]([S:4][CH2:5][CH2:6][C:7]([OH:9])=[O:8])(=[O:3])[CH3:2].[C:10](O)(=[O:13])[CH2:11][OH:12].C(N(CC)CC)C>O1CCCC1>[C:1]([S:4][CH2:5][CH2:6][C:7]([O:9][C:11](=[O:12])[CH2:10][OH:13])=[O:8])(=[O:3])[CH3:2]参加物
実験手順
3-(Acetylthio)propanoic acid (2.96 g) and 1,1'-carboxyldiimidazole (3.24 g) are dissolved in 20 ml of dry tetrahydrofuran with stirring at room temperature. After twenty minutes, a solution of glycolic acid (1.52 g) and 2.80 ml of triethylamine in 15 ml of dry tetrahydrofuran are added. The reaction mixture is stored overnight at room temperature. The tetrahydrofuran is removed in vacuo, the crude residue taken up into ethyl acetate, washed with 1N hydrochloric acid and three times with water, dried over magnesium sulfate and the O-(3-acetylthiopropanoyl)glycolic acid is concentrated to dryness in vacuo, yield 3.9 g. This is dissolved in ether and dicyclohexylamine is added. The dicyclohexylamine salt precipitates, yield 2.85 g.; m.p. 150-157° . The salt is converted to the free acid by adding to ethyl acetate and adding 10% potassium bisulfate solution, yield 1.5 g.
後処理
- waitAfter twenty minutes
- customThe tetrahydrofuran is removed in vacuo
- washwashed with 1N hydrochloric acid and three times with water
- dry with materialdried over magnesium sulfate
- concentrationthe O-(3-acetylthiopropanoyl)glycolic acid is concentrated to dryness in vacuo, yield 3.9 g
- dissolutionThis is dissolved in ether
- additiondicyclohexylamine is added
- customThe dicyclohexylamine salt precipitates
- additionby adding to ethyl acetate
- additionadding 10% potassium bisulfate solution, yield 1.5 g
出典と根拠
- ORDレコード
- ord-40ea0f83f3e74390bba517a8ce795050
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04611002
反応ノート
読み込み中…