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Ammonia → 2-Amino-3,6-dichloro-5-trifluoromethylpyridine

HRID 1290140
ノート
印刷プレビュー

反応式

HRID 1290140 の反応式
[NH3:1].[Cl:2][C:3]1[C:4](OC)=[N:5][C:6]([Cl:13])=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1>CO>[NH2:1][C:4]1[C:3]([Cl:2])=[CH:8][C:7]([C:9]([F:12])([F:11])[F:10])=[C:6]([Cl:13])[N:5]=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 222AmmoniaHCID 186895102,5-Dichloro-6-methoxy-3-trifluoromethylpyridine

生成物 1

HCID 130641542-Amino-3,6-dichloro-5-trifluoromethylpyridine収率 28.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

12.4 g (0.73 mol) of gaseous ammonia were injected into a stirred mixture of 12.8 g (0.052 mol) of 3,6-dichloro-2-methoxy-5-trifluoromethylpyridine in 100 ml of methanol in an autoclave at 140° C., during which process the pressure climbed up to 200 bar. After half an hour, no starting material was detected in a sample. The reaction solution was concentrated and partitioned between methylene chloride and water. After drying, concentration, trituration of the residue with n-pentane, filtration with suction and drying, 3.4 g (28% of theory) of 2-amino-3,6-dichloro-5-trifluoromethylpyridine of m.p. 110°-112° C. were obtained. HPLC analysis revealed that the concentrated pentane filtrate (5 g) was composed of a further 19% of 2-amino-3,6-dichloro-5-trifluoromethylpyridine and 5 other compounds.

後処理

  1. waitAfter half an hour
  2. concentrationThe reaction solution was concentrated
  3. custompartitioned between methylene chloride and water
  4. customAfter drying
  5. concentrationconcentration, trituration of the residue
  6. filtrationwith n-pentane, filtration with suction
  7. customdrying

出典と根拠

ORDレコード
ord-b6e3bef9bf9a47e39e1d9968666e2f33
出典データセット
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05750705

反応ノート

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