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Hydrogen Bromide → 4-(2-Oxo-1-cyclopentylidenemethyl)phenylacetic acid

HRID 1902759
ノート
印刷プレビュー

反応式

HRID 1902759 の反応式
[O:1]=[C:2]1[CH2:6][CH2:5][CH2:4][C:3]1=[CH:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][C:15]([O:17]CC)=[O:16])=[CH:10][CH:9]=1.Br>O1CCOCC1>[O:1]=[C:2]1[CH2:6][CH2:5][CH2:4][C:3]1=[CH:7][C:8]1[CH:9]=[CH:10][C:11]([CH2:14][C:15]([OH:17])=[O:16])=[CH:12][CH:13]=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 260Hydrogen BromideHCID 54231923Ethyl 4-(2-oxo-1-cyclopentylidenemethyl)phenylacetate

生成物 1

HCID 541547854-(2-Oxo-1-cyclopentylidenemethyl)phenylacetic acid

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

A mixture of 0.4 g of ethyl 4-(2-oxo-1-cyclopentylidenemethyl)phenylacetate in 100 ml of a 10% aqueous solution of hydrobromic acid and 10 ml of dioxane was heated under reflux for 1 hour. After cooling, the reaction mixture was extracted with ether, an ether layer was washed with water and dried. The ether was distilled off and the residual oily substance was distilled under reduced pressure to give 0.1 g of an oily substance having a boiling point of 205°-210° C./0.25 mmHg.

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

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 1 hour
  3. temperatureAfter cooling
  4. extractionthe reaction mixture was extracted with ether
  5. washan ether layer was washed with water
  6. customdried
  7. distillationThe ether was distilled off
  8. distillationthe residual oily substance was distilled under reduced pressure
  9. customto give 0.1 g of an oily substance

出典と根拠

ORDレコード
ord-92f1a69b01de4300bd525b2238f39689
出典データセット
uspto-grants-1982_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04365076

反応ノート

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