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Methanol → (3-Bromo-5-fluorophenyl)methanol

HRID 391425
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HRID 391425 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([F:11])[CH:10]=1)[C:5](O)=[O:6].O1CCCC1.B.CO>O1CCCC1.C(OCC)(=O)C>[Br:1][C:2]1[CH:3]=[C:4]([CH2:5][OH:6])[CH:8]=[C:9]([F:11])[CH:10]=1
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참가 물질

6

반응물 3

HCID 887MethanolHCID 2723981Borane;tetrahydrofuranHCID 27733393-Bromo-5-fluorobenzoic acid

생성물 1

HCID 2769402(3-Bromo-5-fluorophenyl)methanol

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매

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온도
0 °C

실험 절차

3-Bromo-5-fluorobenzoic acid (1.0 g, 4.52 mmol) was suspended in tetrahydrofuran (8 mL) and cooled to 0° C. To this solution was added borane tetrahydrofuran complex (1 M in tetrahydrofuran, 9 mL, 9.0 mmol) cautiously over 15 min. The reaction mixture was allowed to warm to room temperature overnight. The mixture was cooled to 0° C., treated with excess methanol, diluted with ethyl acetate, washed with 1 N sodium hydroxide (2×), then brine (2×), dried over sodium sulfate, and concentrated to afford 0.88 g (95%) as a white powder. 1H-NMR (CDCl3, 500 MHz) 7.29 (s, 1H), 7.16 (d, J=7.9 Hz, 1H), 7.03 (d, J=9.2 Hz, 1H), 4.66 (s, 2H).

후처리

  1. temperatureto warm to room temperature overnight
  2. temperatureThe mixture was cooled to 0° C.
  3. washwashed with 1 N sodium hydroxide (2×)
  4. dry with materialbrine (2×), dried over sodium sulfate
  5. concentrationconcentrated
  6. customto afford 0.88 g (95%) as a white powder

출처 및 근거

ORD 기록
ord-1ce982a56fdd4bfd8710c0853567e76c
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08383821B2

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