7-(2,6-Dichloro-4-nitrophenoxy)-2,2-dimethyl-2,3-dihydro-1-benzofuran → HCID 13246037、化合物
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([N+:21]([O-])=O)[CH:5]=[C:6]([Cl:20])[C:7]=1[O:8][C:9]1[C:17]2[O:16][C:15]([CH3:19])([CH3:18])[CH2:14][C:13]=2[CH:12]=[CH:11][CH:10]=1.[H][H]>C1(C)C=CC=CC=1.[Pt]>[Cl:20][C:6]1[CH:5]=[C:4]([CH:3]=[C:2]([Cl:1])[C:7]=1[O:8][C:9]1[C:17]2[O:16][C:15]([CH3:18])([CH3:19])[CH2:14][C:13]=2[CH:12]=[CH:11][CH:10]=1)[NH2:21]参加物
実験手順
To a solution of 29.2 g of 3,5-dichloro-4-(2,3-dihydro-2,2-dimethyl-7-benzofuranyloxy)-1-nitrobenzene in 500 ml of toluene was added 2.3 g of 5% platinum on carbon catalyst. This mixture was then charged into a 1 L rocking Parr reactor. The reactor was purged twice with nitrogen then twice with hydrogen, then finally filled with hydrogen to a pressure of 100 psig. The hydrogen pressure was maintained between 75 and 100 psig during the course of the reaction. After hydrogen uptake ceased, the reaction mixture was removed from the reactor. This was filtered through celite. Removal of the solvents afforded 23.95 g of off-white crystals. mp 140°-145° C. NMR (CDCl3): 1.53 (s, 6H), 3.03 (s, 2H), 3.70 (broad s, 2H), 6.2-7.0 (M, 5H, contains singlet at 6.62).
後処理
- additionThis mixture was then charged into a 1 L
- customThe reactor was purged twice with nitrogen
- additiontwice with hydrogen, then finally filled with hydrogen to a pressure of 100 psig
- temperatureThe hydrogen pressure was maintained between 75 and 100 psig
- customduring the course of the reaction
- customthe reaction mixture was removed from the reactor
- filtrationThis was filtered through celite
- customRemoval of the solvents
出典と根拠
- ORDレコード
- ord-1132b06db1084be1827617c6f9096f9a
- 出典データセット
- uspto-grants-1987_05
- 特許番号
- US04665097
反応ノート
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