Water → 2-[2-(Heptafluoropropoxy)-tetrafluoroethyl]-ethyl alcohol

HRID 640781

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HRID 640781 반응식
[C:1]([O:11][C:12]([C:15]([CH2:18][CH2:19]I)([F:17])[F:16])([F:14])[F:13])([C:4]([C:7]([F:10])([F:9])[F:8])([F:6])[F:5])([F:3])[F:2].CNC=[O:24].O>CCOCC>[C:1]([O:11][C:12]([C:15]([CH2:18][CH2:19][OH:24])([F:17])[F:16])([F:14])[F:13])([C:4]([C:7]([F:10])([F:9])[F:8])([F:6])[F:5])([F:3])[F:2]

참가 물질

5

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온도
150 °C

실험 절차

A mixture of C3F7OCF2CF2CH2CH2I (300 g, 0.68 mol, prepared as described above) and N-methyl-formamide (300 mL), was heated to 150° C. for 26 h. Then the reaction was cooled to 100° C., followed by the addition of water to separate the crude ester. Ethyl alcohol (77 mL) and p-toluene sulfonic acid (2.59 g) were added to the crude ester, and the reaction was stirred at 70° C. for 15 minutes. Then ethyl formate and ethyl alcohol were distilled out to give a crude product. The crude product was dissolved in ether, washed with aqueous sodium sulfite, water, and brine in turn, then dried over magnesium sulfate. The product was then distilled to give 199 g of C3F7OCF2CF2CH2CH2OH in 85% yield. The boiling point was 71-73° C. at 40 mm Hg (5.3 kPa).

후처리

  1. temperatureThen the reaction was cooled to 100° C.
  2. customto separate the crude ester
  3. additionEthyl alcohol (77 mL) and p-toluene sulfonic acid (2.59 g) were added to the crude ester
  4. distillationThen ethyl formate and ethyl alcohol were distilled out
  5. customto give a crude product
  6. washwashed with aqueous sodium sulfite, water, and brine in turn
  7. dry with materialdried over magnesium sulfate
  8. distillationThe product was then distilled

출처 및 근거

ORD 기록
ord-98e403abe9bd4d809b345f0ec07ae498
출처 데이터셋
uspto-grants-2010_04
특허 번호
US07692035B2

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