Trifluoroacetic acid → 1-(1-Azido-1-methylethyl)-3,5-difluorobenzene

HRID 1808209

반응식

HRID 1808209 반응식
[NH:1]=[N+:2]=[N-:3].[F:4][C:5]1[CH:6]=[C:7]([C:12](O)([CH3:14])[CH3:13])[CH:8]=[C:9]([F:11])[CH:10]=1.C(O)(C(F)(F)F)=O.[OH-].[Na+]>C(Cl)(Cl)Cl>[N:1]([C:12]([C:7]1[CH:8]=[C:9]([F:11])[CH:10]=[C:5]([F:4])[CH:6]=1)([CH3:14])[CH3:13])=[N+:2]=[N-:3]

참가 물질

6

반응 조건

온도
-5 °C

실험 절차

Hydrogen azide (2M in toluene, 1.5 mol) was added to the solution of 2-(3,5-difluoro-phenyl)-propan-2-ol (Preparation 50, 145 g, 0.84 mol, 1 eq) in chloroform (1 L) and the content of the flask was cooled to −5° C. The mixture of TFA (2.5 mol, 2.98 eq) with chloroform (1:1) was added dropwise at such a rate to keep the internal temperature below −5° C. After the addition was complete, the reaction mixture was allowed to warm to room temperature and stirring was continued for 20 h. The reaction was poured into 2M sodium hydroxide and layers were separated. The aqueous phase was extracted two times with chloroform and combined organic extracts were washed with brine and dried over anhydrous magnesium sulfate. After removal of the solvent, the title compound was used in the next step without further purification (171 g, 0.87 mol, 100%).

후처리

  1. additionwas added dropwise at such a rate
  2. customthe internal temperature below −5° C
  3. additionAfter the addition
  4. temperatureto warm to room temperature
  5. customwere separated
  6. extractionThe aqueous phase was extracted two times with chloroform
  7. washwere washed with brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. customAfter removal of the solvent
  10. customthe title compound was used in the next step without further purification (171 g, 0.87 mol, 100%)

출처 및 근거

ORD 기록
ord-c707ead22b7345c08a5019d8b7e68bc3
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08357711B2

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