Potassium Carbonate → Ethyl 7-(3-benzyloxypropoxy)-chromane-2-carboxylate
反応式
[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[O:9]2)=[CH:4][CH:3]=1.Br[CH2:18][CH2:19][CH2:20][O:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.C(=O)([O-])[O-].[K+].[K+]>[I-].C([N+](CCCC)(CCCC)CCCC)CCC.CC(C)=O>[CH2:22]([O:21][CH2:20][CH2:19][CH2:18][O:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[O:9]2)=[CH:4][CH:3]=1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1参加物
6
実験手順
To a 200 ml acetone solution of ethyl 7-hydroxychromane-2-carboxylate (9.18 g, 41.3 mmol) was added benzyl 3-bromopropyl ether (14.2 g, 62.0 mmol), powdered potassium carbonate (11.4 g, 82.5 mmol), and tetrabutylammonium iodide (1.53 g, 4 mmol). The resulting suspension was heated to reflux overnight. Acetone was removed under reduced pressure, diluted with AcOEt and sat. NH4Claq. The organic layer was separated, and the aqueous layer was extracted twice with AcOEt. The combined organic layers were dried over anhydrous Na2SO4, filtered, concentrated, and chromatographed on silica gel eluting with 10% AcOEt/hexanes to give the title compound 10.1 g (66%).
後処理
- temperatureThe resulting suspension was heated
- temperatureto reflux overnight
- customAcetone was removed under reduced pressure
- additiondiluted with AcOEt and sat. NH4Claq
- customThe organic layer was separated
- extractionthe aqueous layer was extracted twice with AcOEt
- dry with materialThe combined organic layers were dried over anhydrous Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customchromatographed on silica gel eluting with 10% AcOEt/hexanes
出典と根拠
- ORDレコード
- ord-4795e508b2ae4b97aa5be6d3ec7ae4b9
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06713508B2
反応ノート
読み込み中…