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Acetic Acid → HCID 59586742, 화합물

HRID 218516
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인쇄 미리보기

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HRID 218516 반응식
[F:1][C:2]1[C:7]([CH:8]([OH:11])[CH2:9][CH3:10])=[CH:6][CH:5]=[CH:4][N:3]=1.S(=O)(=O)(O)O.[OH-].[Na+].[C:19](O)(=[O:21])[CH3:20]>>[C:19]([O:11][CH:8]([C:7]1[C:2]([F:1])=[N:3][CH:4]=[CH:5][CH:6]=1)[CH2:9][CH3:10])(=[O:21])[CH3:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 176Acetic AcidHCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 595867223-Pyridinemethanol, alpha-ethyl-2-fluoro-

생성물 1

HCID 59586742HCID 59586742, 화합물

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온도
130 °C

실험 절차

2.75 g (17.7 mmol) of the product from example 48A are dissolved in 12 ml of glacial acetic acid and admixed with 4 ml of concentrated sulfuric acid. The mixture is heated to 130° C. for 30 min and, after cooling, stirred into ice-water. A pH of 8 is established with sodium hydroxide solution, and then extraction is effected with dichloromethane. The combined organic phases are dried over sodium sulfate and concentrated cautiously. This affords 3.30 g (94% of theory) of the title compound, which is converted further without purification.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureafter cooling
  2. extractionextraction
  3. dry with materialThe combined organic phases are dried over sodium sulfate
  4. concentrationconcentrated cautiously
  5. customThis affords 3.30 g (94% of theory) of the title compound, which is converted further without purification

출처 및 근거

ORD 기록
ord-6843322b8014429680fa5a07fc455713
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08198267B2

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