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

HRID 1902759
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반응식

HRID 1902759 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 54231923Ethyl 4-(2-oxo-1-cyclopentylidenemethyl)phenylacetate

생성물 1

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

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-92f1a69b01de4300bd525b2238f39689
출처 데이터셋
uspto-grants-1982_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04365076

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