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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68347Erstellt: 27. Oktober 2026

Boron trifluoride etherate → Tert-butyl 5,5,5-trifluoropentanoate

https://huagongshe.com/reaction/68347

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron trifluoride etherateHCID 8000—
EduktSodium BicarbonateHCID 516892—
EduktTert-butyl 2,2,2-trichloroethanimidateHCID 2734700—
Edukt5,5,5-trifluoropentanoic AcidHCID 2782446—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktTert-butyl 5,5,5-trifluoropentanoateHCID 8667136998,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of 5,5,5-trifluoropentanoic acid (5 g, 32.0 mmol) in THF (30 mL) and hexane (30 mL) at 0° C., was added tert-butyl 2,2,2-trichloroacetimidate (11.46 mL, 64.1 mmol). The mixture was stirred for 15 min at 0° C. Boron trifluoride etherate (0.406 mL, 3.20 mmol) was added and the reaction mixture was allowed to warm to room temperature overnight. To the clear reaction mixture was added solid NaHCO3 (5 g) and stirred for 30 min. The mixture was filtered through MgSO4 and washed with hexanes (200 mL). The solution was allowed to rest for 45 min, and the resulting solid material was removed by filtering on the same MgSO4 filter again, washed with hexanes (100 mL) and concentrated under reduced pressure without heat. The volume was reduced to about 30 mL, filtered through a clean fritted funnel, washed with hexane (5 mL), and then concentrated under reduced pressure without heat. The resulting neat oil was filtered through a 0.45 μm nylon membrane filter disk to provide tert-butyl 5,5,5-trifluoropentanoate (6.6 g, 31.4 mmol 98% yield) as a colorless oil: 1H NMR (400 MHz, CDCl3) δ ppm 1.38 (s, 9H) 1.74-1.83 (m, 2H) 2.00-2.13 (m, 2H) 2.24 (t, J=7.28 Hz, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822454B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-2a9078c6afe84878bf4b0b6bb43b8e34
Quellennotizuspto-grants-2014_09