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Ammonium Chloride → 1-(2-Bromo-6-fluoro-phenyl)-propan-1-ol

HRID 251650
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HRID 251650 반응식
[CH3:1][CH2:2][Mg+].[Br-].[Br:5][C:6]1[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[C:7]=1[CH:8]=[O:9].[NH4+].[Cl-]>C1COCC1>[Br:5][C:6]1[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[C:7]=1[CH:8]([OH:9])[CH2:2][CH3:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 224739772-Bromo-6-fluorobenzaldehydeHCID 178461630HCID 178461630, 화합물

생성물 1

HCID 580898611-(2-Bromo-6-fluoro-phenyl)-propan-1-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
-78 °C

실험 절차

A solution of EtMgBr (35 mL, 35 mmol) in TH-F (1 M) is added dropwise to a solution of 2-bromo-6-fluoro-benzaldehyde (7 g, 34.5 mmol) in THF at −78° C. The mixture is stirred for 1 hour at −78° C. Saturated NH4Cl is added dropwise to the mixture which is subsequently warmed to room temperature and stirred for 1 hour. The organic layer is separated, extracted with THF (3×100 mL. The combined organic layers are washed with brine, dried and solvent is removed in vacuo. The crude product is purified by flash chromatography (5% EtOAc/hexanes) to obtain 1-(2-bromo-6-fluoro-phenyl)-propan-1-ol.

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후처리

  1. temperatureis subsequently warmed to room temperature
  2. stirringstirred for 1 hour
  3. customThe organic layer is separated
  4. extractionextracted with THF (3×100 mL
  5. washThe combined organic layers are washed with brine
  6. customdried
  7. customsolvent is removed in vacuo
  8. customThe crude product is purified by flash chromatography (5% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-74c3ef9f77b5479dab8a6a56be6a5760
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863454B2

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