반응식
[C:1]12([C:11]3[CH:12]=[C:13]([CH:29]=[CH:30][C:31]=3[O:32][Si:33]([C:36]([CH3:39])([CH3:38])[CH3:37])([CH3:35])[CH3:34])[C:14]([O:16][C:17]3[CH:28]=[CH:27][C:20]([C:21]([O:23]CC=C)=[O:22])=[CH:19][N:18]=3)=[O:15])[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.C([SnH](CCCC)CCCC)CCC.Cl>O1CCCC1.[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[C:1]12([C:11]3[CH:12]=[C:13]([CH:29]=[CH:30][C:31]=3[O:32][Si:33]([C:36]([CH3:39])([CH3:38])[CH3:37])([CH3:34])[CH3:35])[C:14]([O:16][C:17]3[CH:28]=[CH:27][C:20]([C:21]([OH:23])=[O:22])=[CH:19][N:18]=3)=[O:15])[CH2:10][CH:5]3[CH2:4][CH:3]([CH2:9][CH:7]([CH2:6]3)[CH2:8]1)[CH2:2]2참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
100 mg of this ester were dissolved in 5 ml of absolute tetrahydrofuran and treated under argon with 104 mg of tetrakis-(triphenylphosphine)-palladium and 61 mg of tributyltin hydride. After stirring at room temperature for 30 min., the reaction mixture was poured on to ice/saturated ammonium chloride solution, acidified with 1N hydrochloric acid and extracted with ethyl acetate. The dark oil obtained after drying and evaporation was purified by chromatography (RP18-LiChroprep, acetonitrile) and recrystallization from ethyl acetate. There were obtained 21 mg of 6-[3-adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoyloxy]-nicotinic acid in colorless crystals, m.p. 188°-190° C.
후처리
- additionthe reaction mixture was poured on to ice/saturated ammonium chloride solution
- extractionextracted with ethyl acetate
- customThe dark oil obtained
- customafter drying
- customevaporation
- customwas purified by chromatography (RP18-LiChroprep, acetonitrile) and recrystallization from ethyl acetate
출처 및 근거
- ORD 기록
- ord-429d4cda5f5a43799ceb5fbb3c399100
- 출처 데이터셋
- uspto-grants-1998_03
- 특허 번호
- US05726191
연결된 노트
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