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Sodium Hydroxide → HCID 53853565、化合物

HRID 2419458
ノート
印刷プレビュー

反応式

HRID 2419458 の反応式
[F:1][C:2]([F:23])([F:22])[C:3]1[CH:8]=[CH:7][C:6]([CH:9]([C:16]2[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=2)[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:5][CH:4]=1.[H][H].[OH-].[Na+]>[Pt]=O.C(O)(=O)C>[F:23][C:2]([F:1])([F:22])[C:3]1[CH:8]=[CH:7][C:6]([CH:9]([C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:16]2[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]2)=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 14798Sodium HydroxideHCID 22748793HCID 22748793、化合物HCID 178418361HCID 178418361、化合物

生成物 1

HCID 53853565HCID 53853565、化合物

試薬・触媒・溶媒 2

HCID 82844Platinum oxide (PtO)触媒HCID 176Acetic Acid溶媒

実験手順

A solution of 15.7 parts of 4-[α-(p-trifluoromethylphenyl)benzyl]pyridine in 250 parts of acetic acid is heated, with agitation, at 47° C. under approximately 4 atmospheres of hydrogen and in the presence of 2 parts of platinum oxide catalyst for 2 hours. The resultant mixture is filtered, and the filtrate is stripped of solvent by vacuum distillation. The residue is poured into 3 volumes of ice water, and the mixture thus obtained is made alkaline with sodium hydroxide. This mixture is then extracted with ether. The ether extract is dried over anhydrous potassium carbonate, filtered, and the ether removed to provide 4-[(4-trifluoromethylphenyl)phenylmethyl]piperidine as an oil.

後処理

  1. filtrationThe resultant mixture is filtered
  2. distillationthe filtrate is stripped of solvent by vacuum distillation
  3. additionThe residue is poured into 3 volumes of ice water
  4. customthe mixture thus obtained
  5. extractionThis mixture is then extracted with ether
  6. extractionThe ether extract
  7. dry with materialis dried over anhydrous potassium carbonate
  8. filtrationfiltered
  9. customthe ether removed

出典と根拠

ORDレコード
ord-257187233b444ed883e2b296b3c73e55
出典データセット
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04105849

反応ノート

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