Dichloromethane → Ethyl 2-Trifluoromethyl-2-methylhexanoate

HRID 1448857Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1448857
[C:1](C(C)(CCCC)C(O)=O)(OCC)=O.ClCCl.F.[F:19][C:20]([F:32])([F:31])[CH:21]([CH2:27][CH2:28][CH2:29][CH3:30])[C:22]([O:24][CH2:25][CH3:26])=[O:23]>CCCCC>[F:19][C:20]([F:31])([F:32])[C:21]([CH3:1])([CH2:27][CH2:28][CH2:29][CH3:30])[C:22]([O:24][CH2:25][CH3:26])=[O:23]

Komponenten

6

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a 90 ml. stainless steel bomb was added 6.6 g. of 2-carboethoxy-2-methylhexanoic acid, 5 ml. of dichloromethane, and 0.4 ml. of 48% hydrofluoric acid. The bomb was sealed with an assembly consisting of a rupture disk (2400-3600 psig) and a needle valve. The bomb was then cooled in a dry ice-acetone bath and evacuated to less than 10 mmHg pressure. Sulfur tetrafluoride (15 g.) was condensed into the bomb from an attached lecture bottle. The needle valve was closed and the bomb was stored in a hood at room temperature for 3 days. After this time, the bomb was immersed to 1/3 of its length in a 60° C. bath. After warming at 60° C. for 3 days, the bomb was cooled and vented. The residual materials were taken up in pentane (250 ml.). The pentane solution was dried (NaF/MgSO4), filtered and distilled to give 3.14 g. (42%) of ethyl 2-trifluoromethylhexanoate, b.p. 79°-81° /20 mmHg.

Aufarbeitung

  1. customThe bomb was sealed with
  2. temperatureThe bomb was then cooled in a dry ice-acetone bath
  3. customevacuated to less than 10 mmHg pressure
  4. customcondensed into the bomb from an attached lecture bottle
  5. customThe needle valve was closed
  6. customwas immersed to 1/3 of its length in a 60° C.
  7. temperaturethe bomb was cooled
  8. dry with materialThe pentane solution was dried (NaF/MgSO4)
  9. filtrationfiltered
  10. distillationdistilled
  11. customto give 3.14 g

Quellen und Nachweise

ORD-Eintrag
ord-2d40e7ebcf2547fe9cb0274abd3740e0
Quelldatensatz
uspto-grants-1980_02
Patentnummer
US04187381

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