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3,3,3-Trifluoropropyne → Ethyl 4-trifluoroprop-1-ynylbenzoate

HRID 2105852
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2105852
[F:1][C:2]([F:6])([F:5])[C:3]#[CH:4].C([Li])CCC.C(O[C:15]1[CH:25]=[C:24](I)[CH:23]=[CH:22][C:16]=1[C:17]([O:19][CH2:20][CH3:21])=[O:18])C>[Cl-].[Zn+2].[Cl-].C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O1CCCC1>[F:1][C:2]([F:6])([F:5])[C:3]#[C:4][C:24]1[CH:23]=[CH:22][C:16]([C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:15][CH:25]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 695783,3,3-TrifluoropropyneHCID 29934691Ethyl 2-ethoxy-4-iodobenzoateHCID 178418339Butyllithium

Produkt 1

HCID 11264994Ethyl 4-trifluoroprop-1-ynylbenzoateAusbeute 62,7 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 3007855ZincchlorideKatalysator
HCID 178418397
HCID 178418397, Verbindung
Katalysator
HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

3,3,3-Trifluoro-1-propyne (approx. 0.6 mL, approx. 6 mmol) was condensed in a flame-dried Schlenk tube immersed in a dry ice/acetone bath. Tetrahydrofuran (3 mL) was added followed by a solution of butyllithium in hexanes (2.15 mL, 3.44 mmol, 1.6 M). After stirring 2.5 h at −78° C., zinc chloride (6.87 mL, 3.44 mmol, 0.5 M solution in tetrahydrofuran) was added to the reaction mixture and the reaction vessel was transferred to an ice-water bath and maintained at 0° C. for 30 min. Ethyl 2-ethoxy-4-iodobenzoate (1.00 g, 3.12 mmol, prepared as described in example 14) and tetrakis(triphenylphosphine)palladium(0) (0.18 g, 0.16 mmol) were then added. The reaction vessel was allowed to warm to room temperature and then after 1 h warmed to 50° C. for 18 h. After cooling, the reaction mixture was partitioned between brine (70 mL) and methylene chloride (2×100 mL), dried over magnesium sulfate and evaporated. Purification of the crude residue by flash column chromatography (silica gel, eluting with 1/1 mixture of methylene chloride and hexanes) gave ethyl 4-trifluoroprop-1-ynylbenzoate as an off-white solid (0.474 g, 53%).

Aufarbeitung

  1. customcondensed in a flame-dried Schlenk tube
  2. customimmersed in a dry ice/acetone bath
  3. customthe reaction vessel was transferred to an ice-water bath
  4. temperaturemaintained at 0° C. for 30 min
  5. temperatureto warm to room temperature
  6. temperatureafter 1 h warmed to 50° C. for 18 h
  7. temperatureAfter cooling
  8. customthe reaction mixture was partitioned between brine (70 mL) and methylene chloride (2×100 mL)
  9. dry with materialdried over magnesium sulfate
  10. customevaporated
  11. customPurification of the crude residue
  12. washby flash column chromatography (silica gel, eluting with 1/1 mixture of methylene chloride and hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-c77a61c3c64748c7befadbbb1bec093e
Quelldatensatz
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07579368B2

Notizen zur Reaktion

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