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 (1Z,4E)-1-hydroxy-5-methoxy-1-(1-methyl-cyclopropyl)-penta-1,4-dien-3-one one (Step 1.7) (111 mmol) and TFA (221 mmol) in toluene (175 mL) was stirred for 15.5 h at rt and then concentrated. The residue was purified using a RediSep® silica gel column to afford the title compound as a white solid. LC-MS: tR=1.48 min, [M+H]+ 151; TLC: Rf=0.26 (EtOAc).
後処理
- concentrationconcentrated
- customThe residue was purified
出典と根拠
- ORDレコード
- ord-e997e3ac78bd4423a715c08ce89eae04
- 出典データセット
- uspto-grants-2012_10
- 特許番号
- US08293753B2
反応ノート
読み込み中…