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Lithium hexamethyldisilazane → 1-(3-Bromo-4-fluorophenyl)-2-[4-(2-fluoroethoxy)-phenyl]ethane-1,2-dione

HRID 643481
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HRID 643481 반응식
C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[Br-].[Br:12][C:13]1[CH:14]=[C:15]([CH:36]=[CH:37][C:38]=1[F:39])[CH2:16][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[F:40][CH2:41][CH2:42][O:43][C:44]1[CH:52]=[CH:51][C:47]([C:48](Cl)=[O:49])=[CH:46][CH:45]=1.I([O-])(=O)(=O)=[O:54].[Na+]>O1CCCC1.O>[Br:12][C:13]1[CH:14]=[C:15]([C:16](=[O:54])[C:48]([C:47]2[CH:51]=[CH:52][C:44]([O:43][CH2:42][CH2:41][F:40])=[CH:45][CH:46]=2)=[O:49])[CH:36]=[CH:37][C:38]=1[F:39]
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참가 물질

7

반응물 4

HCID 2733832Lithium hexamethyldisilazaneHCID 23667635Sodium periodateHCID 450818234-(2-Fluoroethoxy)benzoyl chlorideHCID 86602228(3-Bromo-4-fluoro-benzyl)triphenylphosphonium bromide

생성물 1

HCID 575312621-(3-Bromo-4-fluorophenyl)-2-[4-(2-fluoroethoxy)-phenyl]ethane-1,2-dione수율 41%

시약·촉매·용매 2

HCID 962Water용매
HCID 8028Tetrahydrofuran용매3회

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온도
-20 °C

실험 절차

A 1.0 M solution of lithium bis(trimethylsilyl)amide in tetrahydrofuran (20 mL, 20 mmol was added at room temperature to a stirred suspension of (3-bromo-4-fluoro-benzyl)triphenylphosphonium bromide (10.6 g, 20 mmol) in tetrahydrofuran (40 mL). The mixture was stirred for 40 minutes, then cooled to −20° C. and treated with 4-(2-fluoroethoxy)benzoyl chloride (4.1 g, 20 mmol) in tetrahydrofuran (40 mL) and stirred for an additional 2 hours while slowly warming to room temperature. The mixture was treated with water (20 mL) and sodium periodate (4.3 g, 20 mmol) then stirred at 50° C. for 18 hours. After cooling to room temperature the mixture was extracted with ethyl acetate. The organic extracts were washed with brine, dried over MgSO4. Evaporation and purification by flash chromatography (hexane/ethyl acetate 9/1) gave a yellow solid (3 g, 41% yield); 1H NMR (400 MHZ, CDCl3) δ 4.25 (m, 1H), 4.32 (m, 1H,) 4.70 (m, 1H), 4.82 (m, 1H), 7.01 (d, 2H), 7.23 (m, 1H), 7.94 (m, 3H), 8.22 (m, 1H); MS m/e (M+CH3COO)− 427; mp 107° C.

후처리

  1. stirringstirred for an additional 2 hours
  2. temperaturewhile slowly warming to room temperature
  3. stirringthen stirred at 50° C. for 18 hours
  4. temperatureAfter cooling to room temperature the mixture
  5. extractionwas extracted with ethyl acetate
  6. washThe organic extracts were washed with brine
  7. dry with materialdried over MgSO4
  8. customEvaporation and purification by flash chromatography (hexane/ethyl acetate 9/1)

출처 및 근거

ORD 기록
ord-48d9a0e0211e4e77837da9b4bc2c7e48
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07700602B2

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