Butyric Acid → 4-(3-Trifluoromethylphenyl)-7-methoxy-1-tetralone
反応式
FC(F)(F)C1C=C(C(C2C=CC(OC)=CC=2)CC(OCC)=O)C=CC=1.[F:26][C:27]([F:49])([F:48])[C:28]1[CH:29]=[C:30]([CH:34]([C:40]2[CH:45]=[CH:44][C:43]([O:46][CH3:47])=[CH:42][CH:41]=2)[CH2:35][CH2:36][C:37]([OH:39])=O)[CH:31]=[CH:32][CH:33]=1.C(#N)CCC.C(O)(=O)CCC.CS(O)(=O)=O.O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O>C(O)CC>[F:49][C:27]([F:48])([F:26])[C:28]1[CH:29]=[C:30]([CH:34]2[C:40]3[C:41](=[CH:42][C:43]([O:46][CH3:47])=[CH:44][CH:45]=3)[C:37](=[O:39])[CH2:36][CH2:35]2)[CH:31]=[CH:32][CH:33]=1参加物
反応物 6
生成物 1
試薬・触媒・溶媒 1
実験手順
Ethyl 3-(3-trifluoromethylphenyl)-3-(4-methoxyphenyl)propionate was converted to 4-(3-trifluoromethylphenyl)-4-(4-methoxyphenyl) butanoic acid by standard methods, viz. reduction of the propionate ester to the propanol (93%) tosylation (81%), conversion to the butyronitrile (67%) and hydrolysis to the butanoic acid (85%), which was obtained as a pale yellow oil. This oil (10 g) was stirred overnight at room temperature in a solution of methanesulphonic acid (100 g) and phosphorus pentoxide (21 g). The mixture was poured onto ice, extracted with ether, the extracts washed with dilute sodium hydroxide, dried (MgSO4) and filtered through a short column of alumina. Removal of the ether gave 4-(3-trifluoromethylphenyl)-7-methoxy-1-tetralone as a pale yellow oil (7.65 g, 81%).
後処理
- customwhich was obtained as a pale yellow oil
- additionThe mixture was poured onto ice
- extractionextracted with ether
- washthe extracts washed with dilute sodium hydroxide
- dry with materialdried (MgSO4)
- filtrationfiltered through a short column of alumina
- customRemoval of the ether
出典と根拠
- ORDレコード
- ord-fc18eb758b874a9fb67c582032c62b39
- 出典データセット
- uspto-grants-1982_03
- 特許番号
- US04322370
反応ノート
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