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

HRID 1447038
ノート
印刷プレビュー

反応式

HRID 1447038 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 8471TriethylamineHCID 54250371HCID 54250371、化合物

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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).

後処理

  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%

出典と根拠

ORDレコード
ord-30f9d9f8fb6a4d89b95b74557cc550cc
出典データセット
uspto-grants-1982_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04315020

反応ノート

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