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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Acetic Acid → Phenol, 4-(2,2-dichloroethenyl)-

HRID 482858
ノート
印刷プレビュー

反応式

HRID 482858 の反応式
O1CCCCC1O[C:8]1[CH:9]=[C:10]([CH:14](OC(=O)C)[C:15]([Cl:18])(Cl)[Cl:16])[CH:11]=[CH:12][CH:13]=1.C(O)(=[O:25])C>[Zn]>[Cl:16][C:15]([Cl:18])=[CH:14][C:10]1[CH:11]=[CH:12][C:13]([OH:25])=[CH:8][CH:9]=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 176Acetic AcidHCID 13324246HCID 13324246、化合物

生成物 1

HCID 5324901Phenol, 4-(2,2-dichloroethenyl)-

試薬・触媒・溶媒 1

HCID 23994Zinc触媒

実験手順

22 g (0.06 mole) of 3-(tetrahydropyranyloxy)-1-(2,2,2-trichloro-1-acetoxyethyl)-benzene were dissolved in 80 ml of glacial acetic acid, 4.6 g (0.07 mole) of zinc dust were added a little at a time, and the mixture was heated at 60°-70° C. for 3 hours. The mixture was cooled and filtered, after which it was introduced into 1.5 liters of water and extracted with ether. The extracts were combined, washed three times with NaHCO3 solution and water, dried end evaporated down, and the residue was taken up in toluene. The solution was filtered over silica gel, and 8.0 g of 4-dichlorovinylphenol were obtained as a wax-like product.

後処理

このページの内容参加物実験手順後処理出典と根拠反応ノート
  1. temperaturethe mixture was heated at 60°-70° C. for 3 hours
  2. temperatureThe mixture was cooled
  3. filtrationfiltered
  4. additionafter which it was introduced into 1.5 liters of water
  5. extractionextracted with ether
  6. washwashed three times with NaHCO3 solution and water
  7. customdried end
  8. customevaporated down
  9. filtrationThe solution was filtered over silica gel

出典と根拠

ORDレコード
ord-1d50582121f442ecbe772e253b86d310
出典データセット
uspto-grants-1986_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04576935

反応ノート

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