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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 5,5,6,6,6-Pentafluorohexanoic acid

HRID 1267736
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HRID 1267736 반응식
S(=O)(=O)(O)[OH:2].[F:6][C:7]([F:18])([C:14]([F:17])([F:16])[F:15])[CH2:8][CH2:9][CH2:10][CH2:11]C#N.[OH2:19]>>[F:6][C:7]([F:18])([C:14]([F:17])([F:16])[F:15])[CH2:8][CH2:9][CH2:10][C:11]([OH:2])=[O:19]
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참가 물질

4

반응물 3

HCID 962Water2회HCID 1118Sulfuric AcidHCID 185462625,5,6,6,6-Pentafluorohexanecarbonitrile

생성물 1

HCID 120170595,5,6,6,6-Pentafluorohexanoic acid수율 85%

실험 절차

Concentrated sulfuric acid (350 ml) was slowly added dropwise to 5,5,6,6,6-pentafluorohexanecarbonitrile (108 g, 577.20 mmol) at 0° C., and the resulting mixture was stirred for 3 hours at room temperature. Water (350 ml) was slowly added dropwise to this mixture at 0° C., followed by heating under reflux for 12 hours. After cooling to room temperature, water was added to the reaction mixture, which was then extracted three times with dichloromethane. The combined organic layers were washed with water and saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate. The solvent was distilled off to give 5,5,6,6,6-pentafluorohexanoic acid (95.8 g, Yield 85%).

후처리

  1. temperatureby heating
  2. temperatureunder reflux for 12 hours
  3. temperatureAfter cooling to room temperature
  4. extractionwas then extracted three times with dichloromethane
  5. washThe combined organic layers were washed with water and saturated aqueous sodium chloride
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationThe solvent was distilled off

출처 및 근거

ORD 기록
ord-016e3135ea034b8c9aac70eef6b191a5
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06552068B1

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