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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Phenethylamine → 2,2,2-Trifluoro-N-(2-phenylethyl)ethan-1-amine

HRID 1640238
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반응식

HRID 1640238 반응식
[F:1][C:2]([F:13])([F:12])[CH2:3]OS(C(F)(F)F)(=O)=O.[CH2:14]([NH2:22])[CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C1(C)C(C)=CC=CC=1>[CH2:14]([NH:22][CH2:3][C:2]([F:13])([F:12])[F:1])[CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1001PhenethylamineHCID 803662,2,2-Trifluoroethyl trifluoromethanesulfonate

생성물 1

HCID 135556072,2,2-Trifluoro-N-(2-phenylethyl)ethan-1-amine

시약·촉매·용매 1

HCID 7237O-Xylene용매

실험 절차

1.9 g (8.3 mmol) 2,2,2-trifluoroethyltrifluoromethanesulphonate were added to 2.0 g (16.5 mmol) phenethylamine in 50 mL xylene and the reaction mixture was refluxed overnight. After cooling the precipitate formed was suction filtered, washed with DIPE and the filtrate washed evaporated down i.vac. The residue was purified by flash chromatography. The product fractions were combined and evaporated down i.vac.

후처리

  1. temperaturethe reaction mixture was refluxed overnight
  2. temperatureAfter cooling the precipitate
  3. customformed
  4. filtrationfiltered
  5. washwashed with DIPE
  6. washthe filtrate washed
  7. customevaporated down i.vac
  8. customThe residue was purified by flash chromatography
  9. customevaporated down i.vac

출처 및 근거

ORD 기록
ord-3b6f770e15b4411da73f674d6141b332
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08110575B2

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