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Ammonia → HCID 67403497、化合物

HRID 906052
ノート
印刷プレビュー

反応式

HRID 906052 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

HCID 67403497HCID 67403497、化合物収率 62%

試薬・触媒・溶媒 2

HCID 11026Titanium isopropoxide触媒
HCID 702
Ethanol
溶媒
2 回

実験手順

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+).

後処理

  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

出典と根拠

ORDレコード
ord-a0689e8a61634b04b0fd15c5211b0bbe
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08012956B2

反応ノート

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