反応式
[SH:1][CH2:2][CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[C:9]1(=[O:15])[O:14][C:12](=[O:13])[CH2:11][CH2:10]1>CN(C1C=CN=CC=1)C.C(#N)C.N1C=CC=CC=1>[SH:1][CH2:2][CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[C:9]([OH:14])(=[O:15])[CH2:10][CH2:11][C:12]([OH:5])=[O:13]参加物
実験手順
As shown in FIG. 2, Ethyl 3-mercaptopropionate (2.95 g, 22 mmol) was added under argon to a stirring solution of succinic anhydride (2.0 g, 20 mmol) and DMAP (122 mg, 1 mmol) in 25 ml of acetonitrile-pyridine (9:1). The reaction mixture was stirred at room temperature overnight. The solution was concentrated under reduced pressure and dried in vacuo. The residue was dissolved in 50 ml of EtOAc. The EtOAc solution was washed with 0.1 N HCl aqueous solution 30 ml×3, H2O×3, dried over anhydrous MgSO4. After filtration, the solution was concentrated to dry under reduced pressure and in vacuo. 1H NMR (CDCl3, 500 MHz) δ 10.23 (s, br), 4.14 (2H, q, J=7.0 Hz, —CH2—CH3), 3.13 (2H, t, J=7.0 Hz, —S—CH2—), 2.88 (2H, t, J=7.0 Hz, —S—CO—CH2—), 2.69 (2H, t, J=7.0 Hz, —S—CH2—CH2—), 2.62 (2H, t, J=7.0 Hz, —CH2—COOH), 1.25 (3H, t, J=7.0 Hz, —CH2—CH3).
後処理
- concentrationThe solution was concentrated under reduced pressure
- customdried in vacuo
- dissolutionThe residue was dissolved in 50 ml of EtOAc
- washThe EtOAc solution was washed with 0.1 N HCl aqueous solution 30 ml×3, H2O×3
- dry with materialdried over anhydrous MgSO4
- filtrationAfter filtration
- concentrationthe solution was concentrated
- customto dry under reduced pressure and in vacuo
出典と根拠
- ORDレコード
- ord-ba250d95f261483b8ef9cdf2da8c3578
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08841408B2
関連ノート
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