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Acetic Acid → 2-(4-Bromo-3-fluorophenyl)pyrrolidine

HRID 415152
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HRID 415152 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH2:9][CH2:10][CH2:11][N:12]=2)=[CH:4][C:3]=1[F:13].[BH3-]C#N.[Na+].C(O)(=O)C>CO>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:9][CH2:10][CH2:11][NH:12]2)=[CH:4][C:3]=1[F:13]
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참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 5003444Sodium cyanoborohydrideHCID 666213385-(4-bromo-3-fluorophenyl)-3,4-dihydro-2H-pyrrole

생성물 1

HCID 534036242-(4-Bromo-3-fluorophenyl)pyrrolidine수율 98%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 5-(4-bromo-3-fluorophenyl)-3,4-dihydro-2H-pyrrole ((12.7 g, 52.7 mmol) in 360 mL methanol was added NaBH3CN (6.6 g, 105 mmol) at 0° C. The resulting solution was adjusted to pH=6 with acetic acid. The reaction mixture was stirred at room temperature overnight. The reaction was quenched with 2 N HCl and the methanol was removed by evaporation. The residue was diluted with water, the aqueous phase adjusted to pH=10 with NaOH, extracted with ethyl acetate, dried by Na2SO4, concentrated and the residue was purified by chromatography on silica gel to give 2-(4-bromo-3-fluorophenyl)pyrrolidine as a yellow solid (12.5 g, yield 98%). LC-MS (ESI) m/z: 244 (M+1)+.

후처리

  1. customThe reaction was quenched with 2 N HCl
  2. customthe methanol was removed by evaporation
  3. additionThe residue was diluted with water
  4. extractionextracted with ethyl acetate
  5. dry with materialdried by Na2SO4
  6. concentrationconcentrated
  7. customthe residue was purified by chromatography on silica gel

출처 및 근거

ORD 기록
ord-90e9127cecf34070a4e5dca854305378
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08088760B2

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