Hydrochloric Acid → 4-(2-Oxopropyl)benzoic acid
反応式
Cl.[C:2]([C:5]1[CH:10]=[CH:9][C:8]([CH:11]=[C:12]([N+]([O-])=O)[CH3:13])=[CH:7][CH:6]=1)([OH:4])=[O:3].[OH2:17]>O1CCOCC1.[Fe]>[CH2:11]([C:8]1[CH:9]=[CH:10][C:5]([C:2]([OH:4])=[O:3])=[CH:6][CH:7]=1)[C:12]([CH3:13])=[O:17]参加物
6
実験手順
Concentrated hydrochloric acid (367 ml) was added dropwise to a mixture of 1-(4-carboxyphenyl)-2-nitroprop-1-ene (61.17 g) and iron powder (61.17 g) in dioxan (500 ml) at reflux. The heating was continued for 1 hour at the end of addition. The solution was cooled, water added, the dioxan evaporated and the residue extracted with chloroform and dried (MgSO4). Removal of the solvent gave a solid which was recrystallised from ethyl acetate to give 26 g of the title compound. τ (d6DMSO) 7.83 (3H, s), 6.14 (2H, s), 2.69 (2H, d, J=9 Hz), 2.05 (2H, d, J=9 Hz).
後処理
- temperatureat reflux
- additionThe heating was continued for 1 hour at the end of addition
- temperatureThe solution was cooled
- customthe dioxan evaporated
- extractionthe residue extracted with chloroform
- dry with materialdried (MgSO4)
- customRemoval of the solvent
- customgave a solid which
- customwas recrystallised from ethyl acetate
出典と根拠
- ORDレコード
- ord-bc39e9d84d004a36aee61b0fb43d99ab
- 出典データセット
- uspto-grants-1984_10
- 特許番号
- US04478849
反応ノート
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