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2-(5-Chloro-2-phenoxyphenyl)acetic acid → 2-Chlorodibenzo[b,f]oxepin-10(11h)-one

HRID 1448463
ノート
印刷プレビュー

反応式

HRID 1448463 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[C:6]([CH2:8][C:9]([OH:11])=O)[CH:7]=1>O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[C:9](=[O:11])[CH2:8][C:6]=2[CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 127651142-(5-Chloro-2-phenoxyphenyl)acetic acid

生成物 1

HCID 127651152-Chlorodibenzo[b,f]oxepin-10(11h)-one収率 73.9%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
120 °C

実験手順

Polyphosphoric acid, 500 grams, is heated to 120° C. and 30.5 grams of (5-chloro-2-phenoxyphenyl)acetic acid, prepared in accordance with the procedure of Example 2, is slowly added under an atmosphere of nitrogen with stirring. The reaction mixture is maintained at 120° C. for a period of about two hours, poured over a mixture of ice and water, and extracted into ethyl ether. The combined ether extracts are washed with water until the water washings appear neutral, extracted with a 2 N solution of sodium hydroxide, washed again with water until the water washings are neutral, dried over anhydrous sodium sulfate and filtered. The dried organic solvent is removed from the filtrate by distillation and the residue distilled in vacuo to yield 21 grams of 2-chlorodibenzo[b,f]oxepin-10(11H)-one having a b.p. of 127°-134° C./0.005 mm Hg. Upon recrystallization from methanol, a compound is obtained having an m.p. of 75°-76° C.

後処理

  1. additionis slowly added under an atmosphere of nitrogen
  2. extractionextracted into ethyl ether
  3. washThe combined ether extracts are washed with water until the water washings
  4. extractionextracted with a 2 N solution of sodium hydroxide
  5. washwashed again with water until the water washings
  6. dry with materialdried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. customThe dried organic solvent is removed from the filtrate by distillation
  9. distillationthe residue distilled in vacuo

出典と根拠

ORDレコード
ord-c53bb3530331409d8c6c9c844a526ba1
出典データセット
uspto-grants-1979_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04180559

反応ノート

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