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4-Bromo-2-fluoro-6-(methylthio)benzoic acid → (4-Bromo-2-fluoro-6-(methylthio)phenyl)methanol

HRID 1916882
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HRID 1916882 반응식
[Br:1][C:2]1[CH:10]=[C:9]([S:11][CH3:12])[C:5]([C:6](O)=[O:7])=[C:4]([F:13])[CH:3]=1>C1COCC1>[Br:1][C:2]1[CH:10]=[C:9]([S:11][CH3:12])[C:5]([CH2:6][OH:7])=[C:4]([F:13])[CH:3]=1
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참가 물질

3

반응물 1

HCID 667970144-Bromo-2-fluoro-6-(methylthio)benzoic acid2회

생성물 1

HCID 66797559(4-Bromo-2-fluoro-6-(methylthio)phenyl)methanol수율 90%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
62.5 °C

실험 절차

To a 20 L flask was charged 4-bromo-2-fluoro-6-(methylthio)benzoic acid (1400 g, 1.0 eq) followed by THF (14 L, 10 vol) under nitrogen. To this solution was added borane-dimethyl sulfide complex (802.41 g, 1000 mL) at 25-28° C. over a period of 30-45 min. The reaction temperature was raised to 60-65° C. over a period of 30-45 min and the temperature maintained until HPLC showed <1% of 4-bromo-2-fluoro-6-(methylthio)benzoic acid (˜3-4 h). On completion of the reaction the mixture was cooled to 10-15° C. over a period of 30-40 min. The reaction was then quenched with methanol (2.1 L, 1.5 vol) over a period of 1 to 1½ h at 10-15° C. The reaction mass was then concentrated under vacuum at 40-50° C./0.4 to 0.7 mbar to 1 to 1.5 volumes. The resultant mixture was dissolved in DCM (8.4 L, 6 vol). The organic layer was washed with an ammonium chloride solution (560 g NH4Cl in 2.8 L water, 2 vol). The phases were separated and the organic layer was washed with 10% NaHCO3 solution (2.8 L, 2 vol), saturated brine solution (2.1 L, 1.5 vol) and water (4.2 L, 3 vol). The organic layer was separated and dried over sodium sulfate (700 g). The sodium sulfate was removed by filtration and washed with DCM (2.8 L, 2 vol). The organic layer was concentrated under vacuum at 40-45° C./0.4 to 0.7 mbar to 1 to 1.2 vol to afford the product which was dried under vacuum at 45-50° C./0.4 to 0.7 mbar. The title product was obtained in 90% yield (1200 g) with 90.07 Area %.

후처리

  1. additionTo this solution was added borane-dimethyl sulfide complex (802.41 g, 1000 mL) at 25-28° C. over a period of 30-45 min
  2. temperaturethe temperature maintained until HPLC
  3. customOn completion of the reaction the mixture
  4. temperaturewas cooled to 10-15° C. over a period of 30-40 min
  5. customThe reaction was then quenched with methanol (2.1 L, 1.5 vol) over a period of 1 to 1½ h at 10-15° C
  6. concentrationThe reaction mass was then concentrated under vacuum at 40-50° C./0.4 to 0.7 mbar to 1 to 1.5 volumes
  7. dissolutionThe resultant mixture was dissolved in DCM (8.4 L, 6 vol)
  8. washThe organic layer was washed with an ammonium chloride solution (560 g NH4Cl in 2.8 L water, 2 vol)
  9. customThe phases were separated
  10. washthe organic layer was washed with 10% NaHCO3 solution (2.8 L, 2 vol), saturated brine solution (2.1 L, 1.5 vol) and water (4.2 L, 3 vol)
  11. customThe organic layer was separated
  12. dry with materialdried over sodium sulfate (700 g)
  13. customThe sodium sulfate was removed by filtration
  14. washwashed with DCM (2.8 L, 2 vol)
  15. concentrationThe organic layer was concentrated under vacuum at 40-45° C./0.4 to 0.7 mbar to 1 to 1.2 vol
  16. customto afford the product which
  17. customwas dried under vacuum at 45-50° C./0.4 to 0.7 mbar

출처 및 근거

ORD 기록
ord-313ea890717c499893e15c2905bb02d0
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08618154B2

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