Butyric Acid → 4-(3-Trifluoromethylphenyl)-7-methoxy-1-tetralone

HRID 2059317노트

반응식

HRID 2059317 반응식
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

참가 물질

8

실험 절차

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%).

후처리

  1. customwhich was obtained as a pale yellow oil
  2. additionThe mixture was poured onto ice
  3. extractionextracted with ether
  4. washthe extracts washed with dilute sodium hydroxide
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered through a short column of alumina
  7. customRemoval of the ether

출처 및 근거

ORD 기록
ord-fc18eb758b874a9fb67c582032c62b39
출처 데이터셋
uspto-grants-1982_03
특허 번호
US04322370

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