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Diethylamine → 2,2,2-TRIFLUOROET AMINE,N,N-DIET

HRID 2119264
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HRID 2119264 반응식
[CH2:1]([NH:3][CH2:4][CH3:5])[CH3:2].C(=O)([O-])[O-].[K+].[K+].[F:12][C:13]([F:24])([F:23])[CH2:14]OS(C(F)(F)F)(=O)=O>O>[CH2:1]([N:3]([CH2:4][CH3:5])[CH2:14][C:13]([F:24])([F:23])[F:12])[CH3:2]
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참가 물질

5

반응물 3

HCID 8021DiethylamineHCID 11430Potassium CarbonateHCID 803662,2,2-Trifluoroethyl trifluoromethanesulfonate

생성물 1

HCID 135100982,2,2-TRIFLUOROET AMINE,N,N-DIET

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Diethyl 2,2,2-trifluoroethylamine was prepared as follows. Into a flask were placed diethylamine (5.5 g) and potassium carbonate (10.0 g). 2,2,2-Trifluoroethyl-trifluoromethanesulfonate (12 g) was slowly added to the flask. Heat was evolved. After addition, the reaction mixture was stirred at room temperature overnight. Approximately 100 mL of water was added and the organic layer was separated and dried over MgSO4. The organic liquid was distilled to receive a fraction (a clear liquid 7.25 g) at 88-89° C. under normal pressure. The clear liquid was sampled and analyzed by 1H and 19F NMR. 1H NMR: δ3.56 (q, 2H, J=9 Hz), 2.65 (q, 2H, J=7 Hz), 1.10 (t, 3H, J=7H); ·F NMR: δ−68.13 (t, 3F, J=9 Hz).

후처리

  1. customInto a flask were placed
  2. temperatureHeat
  3. additionAfter addition
  4. customthe organic layer was separated
  5. dry with materialdried over MgSO4
  6. distillationThe organic liquid was distilled
  7. customat 88-89° C.
  8. aliquotThe clear liquid was sampled

출처 및 근거

ORD 기록
ord-efff28170c394105a79719e9fb428be0
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06685793B2

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