Trifluoroacetic acid → 2-(1-Methylcyclopropyl)-4H-pyran-4-one
反応式
O[C:2]([C:10]1([CH3:13])[CH2:12][CH2:11]1)=[CH:3][C:4](=[O:9])[CH:5]=[CH:6][O:7]C.C(O)(C(F)(F)F)=O>C1(C)C=CC=CC=1>[CH3:13][C:10]1([C:2]2[O:7][CH:6]=[CH:5][C:4](=[O:9])[CH:3]=2)[CH2:11][CH2:12]1参加物
4
実験手順
A mixture of 1-hydroxy-5-methoxy-1-(1-methyl-cyclopropyl)-penta-1,4-dien-3-one (Step 40.7) (1.07 g, 5.9 mmol) and TFA (0.9 mL, 11.7 mmol, 2 eq) in toluene (50 mL) is stirred for 14 h at rt and concentrated. Purification of the residue by silica gel column chromatography (Hex/EtOAc, 1:0→3:7) provides 442 mg of the title compound as a red solid: ESI-MS: 151.1 [M+H]+; tR=2.89 min (System 1); TLC: Rf=0.19 (Hex/EtOAc, 1:1).
後処理
- concentrationconcentrated
- customPurification of the residue by silica gel column chromatography (Hex/EtOAc, 1:0→3:7)
出典と根拠
- ORDレコード
- ord-61b4b9e82e5645efa4d0b790d407c259
- 出典データセット
- uspto-grants-2015_01
- 特許番号
- US08940771B2
反応ノート
読み込み中…