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Phosphorus oxychloride → 2-(4-Trifluoromethylphenyl)-4-chloromethyl-5-methyloxazole

HRID 479130
ノート
印刷プレビュー

反応式

HRID 479130 の反応式
[CH3:1][C:2]1[N+:3]([O-])=[C:4]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][CH:9]=2)[O:5][C:6]=1[CH3:7].O=P(Cl)(Cl)[Cl:21]>C(Cl)Cl>[Cl:21][CH2:1][C:2]1[N:3]=[C:4]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][CH:9]=2)[O:5][C:6]=1[CH3:7]
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 24813Phosphorus oxychlorideHCID 10515280Oxazole, 4,5-dimethyl-2-[4-(trifluoromethyl)phenyl]-, 3-oxide

生成物 1

HCID 102363332-(4-Trifluoromethylphenyl)-4-chloromethyl-5-methyloxazole

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

18.5 g of the above prepared 4,5-dimethyl-2-(4-trifluoromethyl-phenyl)-oxazole 3-oxide (72 mmol) was dissolved in 250 ml of CH2Cl2 and treated with 7.909 ml of POCl3 (86.4 mmol). The reaction mixture was refluxed over night and then quenched by carefully pouring onto crashed ice/3N NaOH. Separation of the layers, additional extraction of the aqueous phase with CH2Cl2 and drying of the combined organic layers over magnesium sulfate left, after evaporation of the solvents, 19.78 g of crude product as light brown crystals, which was used as such for the next step.

後処理

  1. temperatureThe reaction mixture was refluxed over night
  2. customquenched
  3. additionby carefully pouring
  4. customSeparation of the layers, additional extraction of the aqueous phase with CH2Cl2
  5. dry with materialdrying of the combined organic layers over magnesium sulfate
  6. waitleft
  7. customafter evaporation of the solvents, 19.78 g of crude product as light brown crystals, which

出典と根拠

ORDレコード
ord-9db056811bf64bd0867c42733b82fe7e
出典データセット
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06642389B2

反応ノート

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