Sulfuric Acid → 7-methoxy-6-methyl-3,4-dihydronaphthalen-1(2H)-one
反応式
COC1C=CC=CC=1C.C1(=O)OC(=O)CC1.[Cl-].[Al+3].[Cl-].[Cl-].[CH3:21][O:22][C:23]1[CH:28]=[C:27]([C:29](=[O:35])[CH2:30][CH2:31][C:32]([OH:34])=O)[CH:26]=[CH:25][C:24]=1[CH3:36].[BH4-].[Na+].[H][H].S(=O)(=O)(O)O>[Pd].C1C=CC=CC=1.C(=S)=S>[CH3:36][C:24]1[CH:25]=[C:26]2[C:27](=[CH:28][C:23]=1[O:22][CH3:21])[C:29](=[O:35])[CH2:30][CH2:31][CH2:32]2.[CH3:36][C:24]1[CH:25]=[C:26]2[C:27]([CH2:29][CH2:30][CH2:31][C:32]2=[O:34])=[CH:28][C:23]=1[O:22][CH3:21]参加物
反応物 7
生成物 2
試薬・触媒・溶媒 3
実験手順
A mixture of 12.2 g. of o-methoxy toluene, 20 g. of succinic anhydride, 27 g. of aluminum chloride, and 250 ml. of carbon disulfide is stirred for four hours; the mixture is poured into 500 g. of ice, and the products are isolated by extraction with benzene. The product, a mixture of 2-methoxy-4-(3'-carboxy-1'-oxopropyl)-toluene and 2-methoxy-5-(3°-carboxy-1'-oxopropyl)-toluene is reduced with sodium borohydride, hydrogenolyzed wiith hydrogen in the presence of palladium charcoal catalyst, cyclized by treatment with concentrated sulfuric acid according to the procedures described in Part A of Example 3 to afford the mixed product 6-methyl-7-methoxy-1-tetralone and 7-methyl-6-methoxy-1-tetralone. The products are separated by distillation and identified by nuclear magnetic resonance.
後処理
- additionA mixture of 12.2 g
- additionthe mixture is poured into 500 g
出典と根拠
- ORDレコード
- ord-ebe46f188569443a91217b585081a863
- 出典データセット
- uspto-grants-1976_08
- 特許番号
- US03978116
反応ノート
読み込み中…