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3-Bromodiphenyl ether → (4-Hydroxy-4-(3-phenoxyphenyl)cyclohexane-1,1-diyl)bis(methylene) bis(4-methylbenzenesulfonate)

HRID 1855028
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HRID 1855028 반응식
Br[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:3]=1.[Li]CCCC.[CH3:20][C:21]1[CH:26]=[CH:25][C:24]([S:27]([O:30][CH2:31][C:32]2([CH2:39][O:40][S:41]([C:44]3[CH:49]=[CH:48][C:47]([CH3:50])=[CH:46][CH:45]=3)(=[O:43])=[O:42])[CH2:37][CH2:36][C:35](=[O:38])[CH2:34][CH2:33]2)(=[O:29])=[O:28])=[CH:23][CH:22]=1>C1COCC1>[CH3:20][C:21]1[CH:26]=[CH:25][C:24]([S:27]([O:30][CH2:31][C:32]2([CH2:39][O:40][S:41]([C:44]3[CH:45]=[CH:46][C:47]([CH3:50])=[CH:48][CH:49]=3)(=[O:43])=[O:42])[CH2:33][CH2:34][C:35]([OH:38])([C:2]3[CH:7]=[CH:6][CH:5]=[C:4]([O:8][C:9]4[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=4)[CH:3]=3)[CH2:36][CH2:37]2)(=[O:28])=[O:29])=[CH:23][CH:22]=1
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참가 물질

5

반응물 3

HCID 961653-Bromodiphenyl etherHCID 88538615(4-Oxocyclohexane-1,1-diyl)bis(methylene) bis(4-methylbenzenesulfonate)HCID 178418339Butyllithium

생성물 1

HCID 90409620(4-Hydroxy-4-(3-phenoxyphenyl)cyclohexane-1,1-diyl)bis(methylene) bis(4-methylbenzenesulfonate)수율 57.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매
2회

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온도
-78 °C

실험 절차

To a solution of 1-bromo-3-phenoxybenzene (0.320 g, 1.29 mmol) in anhydrous THF (10 mL) at −78° C. was added n-BuLi (0.804 mL of a 1.6 M solution in hexanes; 1.286 mmol). The reaction was stirred at −78° C. for 0.5 h and a solution of (4-oxocyclohexane-1,1-diyl)bis(methylene) bis(4-methylbenzenesulfonate) (0.5 g, 1.07 mmol) in THF (5 mL) was then added dropwise. The reaction mixture was slowly warmed to rt and stirred overnight. The reaction was quenched with sat′d aq NH4Cl and diluted with water. The mixture was extracted with EtOAc. The organic layer was dried (Na2SO4) and concentrated in vacuo. The crude oil was purified by flash chromatography on SiO2 (0 to 50% EtOAc:hexanes) to afford the title compound (0.39 g, 57% yield) as a white foam. 1H NMR (500 MHz, CDCl3) δ 7.78 (t, J=8.6 Hz, 4H), 7.41-7.33 (m, 6H), 7.29 (dd, J=11.4, 5.0 Hz, 1H), 7.16-7.10 (m, 1H), 7.08-6.99 (m, 4H), 6.89-6.84 (m, 1H), 4.01 (s, 2H), 3.81 (s, 2H), 2.49 (s, 3H), 2.45 (s, 3H), 1.75-1.47 (m, 8H).

후처리

  1. temperatureThe reaction mixture was slowly warmed to rt
  2. stirringstirred overnight
  3. customThe reaction was quenched with sat′d aq NH4Cl
  4. additiondiluted with water
  5. extractionThe mixture was extracted with EtOAc
  6. dry with materialThe organic layer was dried (Na2SO4)
  7. concentrationconcentrated in vacuo
  8. customThe crude oil was purified by flash chromatography on SiO2 (0 to 50% EtOAc:hexanes)

출처 및 근거

ORD 기록
ord-26e28c72872a4cc8bcce3e416754266f
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08962660B2

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