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

HRID 910820

反応式

HRID 910820 の反応式
[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]

参加物

5

反応条件

温度
150 °C

実験手順

A mixture of C3F7OCF2CF2CH2CH2I (300 g, 0.68 mol) and N-methyl-formamide (300 mL), was heated to 150° C. for 26 hours. 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 mmHg (5320 Pa).

後処理

  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

出典と根拠

ORDレコード
ord-d491a4040e7a471c94ab4f601abb51a4
出典データセット
uspto-grants-2011_09
特許番号
US08022238B2

関連ノート

読み込み中…