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3-Fluoroanisole → 2-Bromo-3-fluoroanisole

HRID 456436
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HRID 456436 반응식
[F:1][C:2]1[CH:3]=[C:4]([O:8][CH3:9])[CH:5]=[CH:6][CH:7]=1.[Li]CCCC.[Br:15]Br>C1COCC1>[Br:15][C:3]1[C:2]([F:1])=[CH:7][CH:6]=[CH:5][C:4]=1[O:8][CH3:9]
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참가 물질

5

반응물 3

HCID 99753-FluoroanisoleHCID 24408BromineHCID 178418339Butyllithium

생성물 1

HCID 27793182-Bromo-3-fluoroanisole

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

The 3-fluoro anisole (15 g, 119 mmol) was placed in THF (300 mL) and cooled to about −78° C., and then n-BuLi (89 mL 1.6 M in hexanes) was added while maintaining the temperature at around −70° C. The mixture was stirred for about 15 minutes, and bromine (18.9 g, 119 mmol) was added over 10 minutes. The mixture was warmed to r.t. and stirred overnight. The mixture was quenched with water, diluted with ether (500 mL) and partitioned between water/ether (1/1 300 mL). The water layer was back extracted with ether (250 mL), and the combined organic fractions were dried, filtered and concentrated. The dark residue was distilled under house vacuum (product 115–130° C.) to recover about 13.8 g of the product as a gray oil (57%).

후처리

  1. temperaturewhile maintaining the temperature at around −70° C
  2. temperatureThe mixture was warmed to r.t.
  3. stirringstirred overnight
  4. customThe mixture was quenched with water
  5. additiondiluted with ether (500 mL)
  6. custompartitioned between water/ether (1/1 300 mL)
  7. extractionThe water layer was back extracted with ether (250 mL)
  8. customthe combined organic fractions were dried
  9. filtrationfiltered
  10. concentrationconcentrated
  11. distillationThe dark residue was distilled under house vacuum (product 115–130° C.)
  12. customto recover about 13.8 g of the product as a gray oil (57%)

출처 및 근거

ORD 기록
ord-5719310a41834985abbfe4ef4bda9c4d
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07186715B2

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