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Triethylamine → (-)-4,5-Dihydro-N-(2,2,2-trifluoro-1-phenylethyl)oxazol-2-amine

HRID 1447038
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HRID 1447038 반응식
[C:1]1([CH:7]([NH:12][C:13]([NH:15][CH2:16][CH2:17]Cl)=[O:14])[C:8]([F:11])([F:10])[F:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(N(CC)CC)C>O>[F:9][C:8]([F:11])([F:10])[CH:7]([NH:12][C:13]1[O:14][CH2:17][CH2:16][N:15]=1)[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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참가 물질

4

반응물 2

HCID 8471TriethylamineHCID 54250371HCID 54250371, 화합물

생성물 1

HCID 6455176(-)-4,5-Dihydro-N-(2,2,2-trifluoro-1-phenylethyl)oxazol-2-amine수율 95%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

7.6 g of N-(α-phenyl trifluoroethyl) N'-(β-Chloroethyl) Urea are suspended in 60 ml water, then 4.3 ml triethylamine are added and the whole mixture is heated to reflux under stirring for 30 mn. The reaction mixture is let to revert to about 20°, the precipitate is separated which is dried, washed with water until the washings are neutral and dried under vacuum--6.3 g 2-[α-(trifluoromethyl) benzylamino] oxazoline are obtained i.e. a yield of 95%. For analytical purpose the compound is recrystallized from isopropanol with a yield of 73%. The analytical sample melts at 162°-168° (sublim).

후처리

  1. temperaturethe whole mixture is heated
  2. temperatureto reflux
  3. customto revert to about 20°
  4. customthe precipitate is separated which
  5. customis dried
  6. washwashed with water until the washings
  7. dry with materialdried under vacuum--6.3 g 2-[α-(trifluoromethyl) benzylamino] oxazoline
  8. customare obtained i.e. a yield of 95%
  9. customFor analytical purpose the compound is recrystallized from isopropanol with a yield of 73%

출처 및 근거

ORD 기록
ord-30f9d9f8fb6a4d89b95b74557cc550cc
출처 데이터셋
uspto-grants-1982_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04315020

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