Dimethylformamide → 4-Formylbenzoic acid
反応式
S(Cl)(Cl)=[O:2].CN(C)[CH:7]=[O:8].[CH:10]1(NC2CCCC2)[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1.C1[CH2:26][O:25]CC1>C1C=CC=CC=1>[C:26]([C:10]1[CH:11]=[CH:12][C:13]([CH:7]=[O:8])=[CH:14][CH:15]=1)([OH:25])=[O:2]参加物
6
実験手順
The acid chloride of 4-carboxybenzaldehyde (7.0 g, 46.5 mmol) was prepared in the same manner as in Example 29 using thionyl chloride (3.5 mL) and dimethylformamide (0.34 mL) in benzene (250 mL). The amide was prepared from the acid chloride in the same manner and using the same workup procedure as in Example 29 using N-cyclohexyl-N-cyclopentyl amine (15.6 g, 93.1 mmol) in THF (150 mL) at 0° C. The crude product was suitable for use without further purification.
後処理
- customat 0° C
- customThe crude product was suitable for use without further purification
出典と根拠
- ORDレコード
- ord-a872729bfc2f4169ba1c28cdba5a239d
- 出典データセット
- uspto-grants-1993_06
- 特許番号
- US05223539
反応ノート
読み込み中…