Potassium tert-butoxide → 2-methyl-2H-pyran-3,5(4H,6H)-dione
反応式
CC(C)([O-])C.[K+].[CH3:7][CH:8]([O:12][CH2:13][C:14]([O:16]C)=O)[C:9](=[O:11])[CH3:10]>C(O)(C)(C)C.CCOCC>[CH3:7][CH:8]1[C:9](=[O:11])[CH2:10][C:14](=[O:16])[CH2:13][O:12]1参加物
5
実験手順
Potassium tert-butoxide in tert-butanol (1 M, 203 mL) and the product from Example 44B (15.5 g, 97 mmol) in ether (55 mL) were processed as described in Example 43C. The residue was purified on silica gel eluting with ethyl acetate:formic acid:water:hexane (200:1:1:200) provided the title compound. 1H NMR (CDCl3) δ 1.48 (d, 3H), 3.43 (d, 1H), 3.92 (d, 1H), 3.97 (q, 1H), 4.04 (d, 1H), 4.44 (d, 1H).
後処理
- customThe residue was purified on silica gel eluting with ethyl acetate:formic acid:water:hexane (200:1:1:200)
出典と根拠
- ORDレコード
- ord-40aaaa9b0f7e4af2afa1164456245a56
- 出典データセット
- uspto-grants-2004_08
- 特許番号
- US06780872B2
反応ノート
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