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Ethanol → 1-(2,2,2-Trifluoroethoxy)-2-Naphthoic Acid

HRID 1973188
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인쇄 미리보기

반응식

HRID 1973188 반응식
[F:1][C:2]([F:20])([F:19])[CH2:3][O:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][C:6]=1[C:15]([O:17]C)=[O:16].[OH-].[K+].C(O)C>O>[F:1][C:2]([F:19])([F:20])[CH2:3][O:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][C:6]=1[C:15]([OH:17])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 14797Potassium HydroxideHCID 21493172Methyl 1-(2,2,2-trifluoroethoxy)naphthalene-2-carboxylate

생성물 1

HCID 214931531-(2,2,2-Trifluoroethoxy)-2-Naphthoic Acid

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 10 g. (35 mmoles) of methyl 1-(2,2,2-trifluoroethoxy)-2-naphthoate, 2.9 g., (42 mmoles) of potassium hydroxide, 50 ml. of ethanol and 40 ml. of water is refluxed for one hour, chilled and acidified. The fluffy precipitate is collected, water washed, and air-dried. It is purified by recrystallization first from chloroform and then from aqueous alcohol, m.p. 171.5°-172° C.

후처리

  1. additionA mixture of 10 g
  2. temperaturechilled
  3. customThe fluffy precipitate is collected
  4. washwater washed
  5. customair-dried
  6. customIt is purified by recrystallization first from chloroform

출처 및 근거

ORD 기록
ord-7aeb48dd48134ebea64d7748f1e929a7
출처 데이터셋
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03996280

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