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Ammonia → HCID 67403497, 화합물

HRID 906052
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HRID 906052 반응식
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([C:9](=O)[CH3:10])=[C:4]([F:12])[CH:3]=1.[NH3:13].[BH4-].[Na+].[OH-].[NH4+]>C(O)C.CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-]>[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([CH:9]([NH2:13])[CH3:10])=[C:4]([F:12])[CH:3]=1
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7

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HCID 222AmmoniaHCID 14923Ammonium HydroxideHCID 4311764Sodium borohydrideHCID 670016231-(4-Bromo-2,6-difluorophenyl)ethan-1-one

생성물 1

HCID 67403497HCID 67403497, 화합물수율 62%

시약·촉매·용매 2

HCID 11026Titanium isopropoxide촉매
HCID 702Ethanol용매2회

실험 절차

To a mixture of 1-(4-bromo-2,6-difluorophenyl)ethanone (450 mg, 0.91 mmol), titanium isopropoxide (1.14 mL, 4.61 mmol) in ethanol (10 mL) was added a solution of 2M ammonia in ethanol (4.8 mL, 9.6 mmol), and the resulting mixture was stirred at room temperature. After 18 hours, sodium borohydride (115 mg, 3.48 mmol) was added and stirring was continued at room temperature for three hours. The reaction mixture was poured into a 2M aqueous ammonium hydroxide solution (100 mL) then filtered. The filtrate was extracted with ethyl acetate (3×50 mL), and the combined extract was washed with water (100 mL), then brine (100 mL), dried over sodium sulfate, filtered and concentrated to give 1-(4-bromo-2,6-difluorophenyl)ethanamine (236 mg, 62% yield), MS (EI) for C8H8BrF2N: 237 (MH+).

후처리

  1. stirringstirring
  2. waitwas continued at room temperature for three hours
  3. filtrationthen filtered
  4. extractionThe filtrate was extracted with ethyl acetate (3×50 mL)
  5. extractionthe combined extract
  6. washwas washed with water (100 mL)
  7. dry with materialbrine (100 mL), dried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a0689e8a61634b04b0fd15c5211b0bbe
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08012956B2

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